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: rs11583978
rs11583978
2 0.925 0.040 1 34864921 downstream gene variant A/C;G snv 0.010 1.000 1 2011 2011
dbSNP: rs4652867
rs4652867
1 1.000 0.040 1 34901689 intron variant G/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs6662980
rs6662980
1 1.000 0.040 1 34894477 intron variant A/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs7541937
rs7541937
1 1.000 0.040 1 34876381 intron variant T/G snv 0.47 0.010 1.000 1 2011 2011