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: rs2288327
rs2288327
1 1.000 0.080 2 178546938 intron variant A/G snv 0.23 0.22 0.700 1.000 3 2018 2018
dbSNP: rs12614435
rs12614435
1 1.000 0.080 2 178624999 intron variant A/G snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs35504893
rs35504893
1 1.000 0.080 2 178556567 non coding transcript exon variant C/T snv 0.24 0.700 1.000 1 2018 2018