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: rs35506085
rs35506085
3 11 2144346 intron variant G/A snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs3741210
rs3741210
2 11 2148310 non coding transcript exon variant A/G snv 0.30 0.700 1.000 1 2019 2019