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: rs7939917
rs7939917
3 0.882 0.040 11 113697374 missense variant C/T snv 2.0E-03 9.2E-03 0.700 1.000 1 2017 2017