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: rs121913555
rs121913555
1 1.000 19 51382430 missense variant A/C snv 1.2E-05 7.0E-06 0.800 1.000 1 2002 2002
dbSNP: rs869312732
rs869312732
1 1.000 19 51380262 missense variant C/T snv 0.700 0