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: rs104894204
rs104894204
4 0.882 0.040 11 19188245 missense variant A/C snv 0.030 1.000 3 2004 2018
dbSNP: rs104894205
rs104894205
3 0.882 0.040 11 19188286 missense variant A/G snv 1.2E-05 5.6E-05 0.010 1.000 1 2018 2018
dbSNP: rs267606753
rs267606753
1 1.000 0.040 11 19188253 missense variant T/C snv 0.010 1.000 1 2018 2018