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: rs11088565
rs11088565
1 21 16101911 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11909251
rs11909251
1 21 16110067 intron variant G/T snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs2823612
rs2823612
1 21 16107233 intron variant T/C snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs2823615
rs2823615
2 21 16110813 intron variant A/T snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs9975788
rs9975788
1 21 16092495 intron variant C/T snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs9983980
rs9983980
1 21 16100046 intron variant C/T snv 0.32 0.700 1.000 1 2012 2012