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: rs1969539
rs1969539
1 11 14017074 intron variant A/G snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs7102710
rs7102710
3 11 14244067 intron variant T/C snv 0.10 0.700 1.000 1 2019 2019