Source: GWASDB

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: rs7076156
rs7076156
0.925 0.120 10 62655424 missense variant A/C;G snv 0.80
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 1 2011 2012
dbSNP: rs10995170
rs10995170
10 62463624 intron variant T/C snv 0.30
CUI: C0021704
Disease: Intelligence
Intelligence
0.800 1.000 1 2012 2012
dbSNP: rs10995245
rs10995245
0.882 0.160 10 62631615 intron variant G/A;C snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.800 1.000 1 2013 2013
dbSNP: rs10995251
rs10995251
1.000 0.120 10 62638706 intron variant C/T snv 0.29
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.800 1.000 1 2012 2012
dbSNP: rs7089814
rs7089814
10 62427805 intron variant C/G;T snv
CUI: C0425782
Disease: Breast size
Breast size
0.800 1.000 1 2012 2012
dbSNP: rs10995190
rs10995190
0.882 0.080 10 62518923 intron variant G/A snv 0.16
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.770 1.000 3 2010 2017
dbSNP: rs10822013
rs10822013
0.851 0.080 10 62492218 intron variant C/T snv 0.42
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.720 1.000 1 2011 2016
dbSNP: rs10995189
rs10995189
1.000 0.080 10 62518422 intron variant G/A snv 0.16
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.700 1.000 1 2010 2010
dbSNP: rs10995190
rs10995190
0.882 0.080 10 62518923 intron variant G/A snv 0.16
CUI: C1268717
Disease: Mammographic Breast Density
Mammographic Breast Density
0.700 1.000 1 2011 2011
dbSNP: rs10995191
rs10995191
1.000 0.080 10 62519115 intron variant C/T snv 0.15
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.700 1.000 1 2010 2010
dbSNP: rs10995194
rs10995194
1.000 0.080 10 62528371 intron variant G/C snv 0.14
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.700 1.000 1 2010 2010
dbSNP: rs10995195
rs10995195
1.000 0.080 10 62528630 intron variant T/C snv 0.18
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.700 1.000 1 2010 2010
dbSNP: rs2077316
rs2077316
10 62465689 intron variant A/C;T snv
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death
0.700 1.000 1 2013 2013
dbSNP: rs2393903
rs2393903
1.000 0.120 10 62620576 intron variant T/A;C snv
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.700 1.000 1 2011 2011
dbSNP: rs4746419
rs4746419
1.000 0.080 10 62515502 intron variant C/G snv 0.15
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.700 1.000 1 2010 2010
dbSNP: rs7071642
rs7071642
1.000 0.040 10 62654300 intron variant G/A snv 0.81
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2012 2012