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: rs11929034
rs11929034
2 3 122560202 intron variant G/A snv 0.14 0.700 1.000 1 2010 2010
dbSNP: rs16833168
rs16833168
2 3 122535800 3 prime UTR variant C/A;G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs17267388
rs17267388
2 3 122548699 intron variant G/A snv 0.14 0.700 1.000 1 2010 2010
dbSNP: rs2270859
rs2270859
3 1.000 0.040 3 122536861 non coding transcript exon variant G/A snv 0.14 0.700 1.000 1 2010 2010