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: rs752669339
rs752669339
1 1.000 10 95610260 missense variant C/G snv 1.2E-05 7.0E-06 0.800 0
dbSNP: rs768323248
rs768323248
2 0.925 0.080 10 95637357 missense variant C/T snv 1.6E-05 7.0E-06 0.700 1.000 1 2015 2015
dbSNP: rs869320690
rs869320690
1 1.000 10 95613755 missense variant A/G snv 0.800 1.000 1 2015 2015