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: rs104894727
rs104894727
4 0.882 0.080 19 55151881 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs397516347
rs397516347
5 0.851 0.120 19 55154157 missense variant C/T snv 4.2E-05 0.700 0
dbSNP: rs397516354
rs397516354
8 0.790 0.120 19 55154094 missense variant C/A;G;T snv 4.0E-05 0.700 0
dbSNP: rs397516357
rs397516357
5 0.851 0.120 19 55151910 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs730881069
rs730881069
2 1.000 0.080 19 55154172 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs104894724
rs104894724
8 0.790 0.120 19 55154146 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2017 2017