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: rs1554261079
rs1554261079
1 1.000 6 158114896 missense variant C/T snv 0.700 1.000 3 2012 2018
dbSNP: rs201941476
rs201941476
1 1.000 6 158116193 missense variant C/G snv 2.4E-05 2.8E-05 0.700 1.000 3 2012 2018