rs10015979
|
1.000 |
0.120 |
4 |
3107715 |
intron variant |
A/G
|
snv
|
|
0.30
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs110501
|
1.000 |
0.120 |
4 |
3223751 |
intron variant |
T/C
|
snv
|
|
0.47
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs11731237
|
1.000 |
0.120 |
4 |
3150086 |
intron variant |
C/T
|
snv
|
|
0.26
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs2071655
|
1.000 |
0.120 |
4 |
3116389 |
intron variant |
T/A;G
|
snv
|
|
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs2269499
|
1.000 |
0.120 |
4 |
3237975 |
intron variant |
C/T
|
snv
|
|
0.24
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs2285086
|
1.000 |
0.120 |
4 |
3087532 |
intron variant |
A/G
|
snv
|
|
0.48
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs2298969
|
1.000 |
0.120 |
4 |
3184517 |
intron variant |
A/G;T
|
snv
|
|
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs2471347
|
1.000 |
0.120 |
4 |
3042708 |
intron variant |
G/A
|
snv
|
|
0.68
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs2798296
|
1.000 |
0.120 |
4 |
3060438 |
intron variant |
A/G
|
snv
|
|
0.44
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs362272
|
1.000 |
0.120 |
4 |
3233253 |
missense variant |
G/A;T
|
snv
|
0.29
|
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs363066
|
1.000 |
0.120 |
4 |
3134226 |
intron variant |
T/A;G
|
snv
|
|
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs363092
|
1.000 |
0.120 |
4 |
3194302 |
intron variant |
A/C;T
|
snv
|
|
0.51
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs363096
|
1.000 |
0.120 |
4 |
3178294 |
splice region variant |
T/C
|
snv
|
0.55
|
0.60
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs3856973
|
1.000 |
0.120 |
4 |
3078446 |
intron variant |
G/A;C
|
snv
|
|
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs6855981
|
1.000 |
0.120 |
4 |
3146549 |
intron variant |
G/A
|
snv
|
|
0.34
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs82333
|
1.000 |
0.120 |
4 |
3223662 |
intron variant |
A/C;G
|
snv
|
|
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs916171
|
1.000 |
0.120 |
4 |
3215088 |
intron variant |
C/G
|
snv
|
0.42
|
0.47
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs71180116
|
1.000 |
0.120 |
4 |
3074877 |
inframe insertion |
GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA/-;GCA;GCAGCA;GCAGCAGCA;GCAGCAGCAGCA;GCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA
|
delins
|
|
0.14
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.700 |
|
0 |
|
|
rs1210554604
|
1.000 |
0.120 |
4 |
3131662 |
missense variant |
G/A
|
snv
|
|
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs13102260
|
1.000 |
0.120 |
4 |
3074678 |
intron variant |
G/A
|
snv
|
|
0.15
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1313770
|
1.000 |
0.120 |
4 |
3056082 |
intron variant |
A/G
|
snv
|
|
0.57
|
Huntington Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
|
0.010 |
1.000 |
1 |
2005 |
2005 |