Source: ALL
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: rs1363819544
rs1363819544
TNF
1 1.000 0.160 6 31577126 synonymous variant A/G snv 7.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs35960726
rs35960726
HAVCR2
2 1.000 0.160 5 157106730 missense variant T/C snv 2.7E-03 2.6E-03 0.010 1.000 1 2018 2018