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: rs4871750
rs4871750
2 8 126889758 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs4871752
rs4871752
1 8 126908341 intron variant G/A snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs7012789
rs7012789
1 8 126904963 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7817717
rs7817717
1 8 126891017 intron variant T/G snv 0.43 0.700 1.000 1 2012 2012