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: rs121913150
rs121913150
1 1.000 0.080 19 7120707 missense variant C/T snv 8.0E-06 7.0E-06 0.800 1.000 5 1992 2013
dbSNP: rs182552223
rs182552223
1 1.000 0.080 19 7141787 missense variant T/C snv 1.2E-04 1.4E-05 0.700 0