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: rs104893836
rs104893836
7 0.790 0.160 4 67754019 missense variant T/C snv 2.8E-03 2.3E-03 0.010 1.000 1 2010 2010
dbSNP: rs1363196459
rs1363196459
3 0.882 0.040 4 147486001 missense variant A/G snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs970697573
rs970697573
3 0.882 0.040 19 19626965 missense variant C/T snv 0.010 1.000 1 2010 2010