Source: ALL
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: rs143913245
rs143913245
GPRC6A
1 1.000 0.040 6 116800741 missense variant A/T snv 1.1E-03 4.6E-03 0.010 1.000 1 2016 2016