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: rs11587735
rs11587735
1 1 117610389 intron variant A/C snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs34754277
rs34754277
1 1 117605270 intron variant T/C snv 0.14 0.700 1.000 1 2016 2016