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: rs11879191
rs11879191
2 1.000 0.040 19 10402235 intron variant G/A;C snv 0.800 1.000 2 2012 2017
dbSNP: rs35164067
rs35164067
2 1.000 0.040 19 10414505 intron variant G/A snv 0.18 0.700 1.000 1 2015 2015