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: rs121913315
rs121913315
5 0.882 0.160 19 1220488 missense variant G/A;T snv 0.800 1.000 1 1999 1999
dbSNP: rs121913323
rs121913323
2 1.000 0.040 19 1220416 stop gained C/T snv 0.700 0
dbSNP: rs137853080
rs137853080
2 1.000 0.040 19 1207058 missense variant T/G snv 0.800 0
dbSNP: rs137853081
rs137853081
2 1.000 0.040 19 1219352 missense variant G/C;T snv 0.800 0