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: rs10045595
rs10045595
1 1.000 0.080 5 167802999 intron variant T/G snv 0.36 0.700 1.000 1 2009 2009
dbSNP: rs172137
rs172137
2 0.925 0.120 5 167604857 intron variant G/A;T snv 0.700 1.000 1 2009 2009