Source: CURATED ×
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: rs28607014
rs28607014
1 1.000 0.040 12 117270806 intron variant C/T snv 0.32 0.700 1.000 2 2017 2019
dbSNP: rs2293052
rs2293052
1 1.000 0.040 12 117277815 intron variant G/A snv 0.28 0.700 1.000 1 2015 2015