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: rs10404876
rs10404876
2 19 12876791 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs11085822
rs11085822
2 19 12874762 synonymous variant A/G snv 0.34 0.34 0.700 1.000 1 2009 2009
dbSNP: rs12609744
rs12609744
2 19 12883326 intron variant T/C snv 0.36 0.700 1.000 1 2009 2009
dbSNP: rs7249143
rs7249143
2 19 12881765 intron variant G/T snv 0.36 0.700 1.000 1 2009 2009