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: rs763862849
rs763862849
1 1.000 0.080 3 53122376 missense variant T/C;G snv 5.2E-05; 4.0E-06 0.800 1.000 2 2008 2009
dbSNP: rs118203913
rs118203913
1 1.000 0.080 3 53123791 missense variant G/A snv 1.6E-05 3.5E-05 0.700 0
dbSNP: rs749968109
rs749968109
1 1.000 0.080 3 53092502 missense variant C/T snv 1.6E-05 0.700 0
dbSNP: rs772820136
rs772820136
1 1.000 0.080 3 53105743 missense variant A/C;G;T snv 8.0E-06 0.700 0
dbSNP: rs796053521
rs796053521
1 1.000 0.080 3 53105738 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs796053522
rs796053522
1 1.000 0.080 3 53092605 missense variant T/C snv 0.700 0
dbSNP: rs913477149
rs913477149
13 0.851 0.160 3 53105728 missense variant T/A;C snv 0.700 0