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: rs10131032
rs10131032
2 1.000 0.040 14 32780875 intron variant G/A snv 9.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs2239647
rs2239647
7 0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 0.010 1.000 1 2019 2019