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: rs12997625
rs12997625
2 2 202105527 intron variant C/T snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs2882485
rs2882485
1 2 202115530 non coding transcript exon variant A/C;G snv 0.42 0.700 1.000 1 2019 2019