Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800553
rs1800553
17 0.742 0.240 1 94008251 missense variant C/T snv 4.7E-03 3.0E-03 0.060 0.833 6 1999 2019
dbSNP: rs1800555
rs1800555
1 1.000 0.040 1 93998061 missense variant C/T snv 1.1E-02 1.0E-02 0.030 0.667 3 2000 2015
dbSNP: rs1800549
rs1800549
2 0.925 0.040 1 94030497 missense variant G/A snv 4.6E-03 1.6E-03 0.010 1.000 1 1999 1999
dbSNP: rs61750120
rs61750120
4 0.882 0.160 1 94042767 missense variant G/A snv 1.2E-04 1.8E-04 0.010 1.000 1 1999 1999
dbSNP: rs61750200
rs61750200
8 0.790 0.080 1 94098928 missense variant G/A;T snv 1.1E-04; 8.0E-06 0.010 1.000 1 1999 1999
dbSNP: rs752160946
rs752160946
1 1.000 0.040 1 94010868 missense variant C/G;T snv 4.0E-06; 2.8E-05 0.010 1.000 1 2015 2015
dbSNP: rs768435443
rs768435443
8 0.807 0.080 1 94055128 missense variant A/G snv 4.0E-06 0.010 1.000 1 2019 2019