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: rs114086406
rs114086406
2 1.000 0.040 6 32374760 intron variant G/A snv 0.700 1.000 1 2017 2017
dbSNP: rs115035678
rs115035678
2 1.000 0.040 6 32381780 intron variant A/T snv 0.700 1.000 1 2017 2017
dbSNP: rs115558405
rs115558405
2 1.000 0.040 6 32368989 intron variant A/G snv 0.700 1.000 1 2017 2017
dbSNP: rs116254153
rs116254153
2 1.000 0.040 6 32371870 5 prime UTR variant T/C;G snv 0.700 1.000 1 2017 2017