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: rs1401419
rs1401419
3 1.000 0.040 11 45858188 intron variant T/C snv 0.39 0.010 1.000 1 2013 2013
dbSNP: rs7945565
rs7945565
1 1.000 0.040 11 45857441 intron variant A/G snv 0.39 0.010 1.000 1 2013 2013