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: rs704364
rs704364
1 1.000 0.040 3 63889058 intron variant A/G snv 0.60 0.700 1.000 1 2019 2019
dbSNP: rs704373
rs704373
1 1.000 0.040 3 63881679 intron variant A/G;T snv 0.700 1.000 1 2018 2018