Source: INFERRED ×
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: rs2466103
rs2466103
1 8 32554786 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs7826312
rs7826312
2 8 32542597 intron variant T/C snv 0.57 0.700 1.000 1 2019 2019