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: rs121908557
rs121908557
23 0.752 0.280 17 63957514 missense variant C/T snv 8.2E-06 1.4E-05 0.040 1.000 4 2008 2019
dbSNP: rs80338962
rs80338962
13 0.742 0.240 17 63941508 missense variant T/C snv 0.040 1.000 4 2002 2018
dbSNP: rs80338957
rs80338957
11 0.776 0.160 17 63957427 missense variant G/A snv 0.010 1.000 1 2018 2018