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: rs397517201
rs397517201
16 0.715 0.214 3 179218307 missense variant A/C,G,T snp 0.700 5 2006 2013
dbSNP: rs121913272
rs121913272
11 0.756 0.321 3 179210192 missense variant T/C,G snp 0.700 4 2004 2013
dbSNP: rs121913274
rs121913274
33 0.626 0.286 3 179218304 missense variant A/C,G,T snp 0.700 1 2013 2013
dbSNP: rs121913273
rs121913273
29 0.638 0.357 3 179218294 missense variant G/A,C snp 0.700 0
dbSNP: rs121913279
rs121913279
68 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 0.700 0