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: rs10507274
rs10507274
2 1.000 0.040 12 116723171 missense variant T/C snv 4.7E-02 4.4E-02 0.700 1.000 1 2018 2018