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: rs1638703
rs1638703
2 1.000 0.040 13 50514220 intron variant G/C snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs6561599
rs6561599
2 1.000 0.040 13 50904782 non coding transcript exon variant C/G snv 0.61 0.700 1.000 1 2018 2018