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: rs121913459
rs121913459
25 0.672 0.160 9 130872896 missense variant C/T snv 0.700 0
dbSNP: rs121913461
rs121913461
5 0.851 0.120 9 130862970 missense variant T/C snv 0.700 0
dbSNP: rs387906516
rs387906516
1 9 130862920 missense variant A/T snv 0.700 0
dbSNP: rs387906517
rs387906517
6 0.827 0.120 9 130862919 missense variant G/A snv 0.700 0