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: rs2247870
rs2247870
1 1.000 0.040 5 90855772 missense variant G/A snv 0.54 0.45 0.700 1.000 2 2017 2019
dbSNP: rs2247419
rs2247419
1 1.000 0.040 5 90859597 intron variant A/G snv 0.57 0.700 1.000 1 2015 2015