Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1999805
rs1999805
1.000 0.120 6 151747229 intron variant G/A snv 0.55
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 3 2008 2009
dbSNP: rs2504063
rs2504063
6 151769572 intron variant A/G snv 0.50
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 2 2009 2009
dbSNP: rs3020333
rs3020333
6 151689119 intron variant A/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 2 2009 2018
dbSNP: rs397509428
rs397509428
1.000 6 152011684 missense variant G/T snv
CUI: C3809250
Disease: ESTROGEN RESISTANCE
ESTROGEN RESISTANCE
0.800 1.000 2 2013 2017
dbSNP: rs2941740
rs2941740
6 151688503 intron variant A/G snv 0.40
CUI: C0005938
Disease: Bone Density
Bone Density
0.800 1.000 1 2009 2009
dbSNP: rs1131692059
rs1131692059
1.000 6 152011740 missense variant G/A snv
CUI: C3809250
Disease: ESTROGEN RESISTANCE
ESTROGEN RESISTANCE
0.800 0
dbSNP: rs796065354
rs796065354
0.882 0.080 6 151944320 missense variant A/G snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.760 1.000 5 2000 2013
dbSNP: rs9383938
rs9383938
0.827 0.160 6 151666222 intron variant G/T snv 0.11
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.720 1.000 1 2011 2014
dbSNP: rs9383938
rs9383938
0.827 0.160 6 151666222 intron variant G/T snv 0.11
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.720 1.000 1 2011 2014
dbSNP: rs1057519827
rs1057519827
6 152011697 missense variant G/C snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 3 2013 2014
dbSNP: rs1057519717
rs1057519717
6 152098785 missense variant T/G snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 2 2013 2013
dbSNP: rs3020331
rs3020331
6 151687645 intron variant C/T snv 0.38
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 2 2009 2009
dbSNP: rs1057519714
rs1057519714
6 152094402 missense variant T/C snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2013 2013
dbSNP: rs1057519715
rs1057519715
1.000 0.080 6 152098779 missense variant T/A snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2013 2013
dbSNP: rs1057519716
rs1057519716
6 152098782 missense variant C/A snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2013 2013
dbSNP: rs10872678
rs10872678
6 151718829 intron variant T/C snv 0.33
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs1101081
rs1101081
6 151711782 intron variant C/T snv 0.26
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2016 2016
dbSNP: rs11155811
rs11155811
6 151756711 intron variant C/T snv 0.44
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs1124674
rs1124674
6 151759600 intron variant T/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs11446767
rs11446767
6 151754327 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTT;TTTTTTTTTT;TTTTTTTTTTTTTTTTT delins
CUI: C0425782
Disease: Breast size
Breast size
0.700 1.000 1 2018 2018
dbSNP: rs1293936
rs1293936
6 151696556 intron variant T/G snv 0.45
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs13192976
rs13192976
6 151991280 intron variant A/T snv 0.16
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2017 2017
dbSNP: rs1336981
rs1336981
6 151761234 intron variant C/T snv 0.74
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs1415193
rs1415193
6 151771503 intron variant T/A snv 0.37
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009
dbSNP: rs1415194
rs1415194
6 151742863 intron variant A/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2009 2009