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: rs768481542
rs768481542
CHD7
1 1.000 0.080 8 60822028 missense variant G/A snv 7.6E-05 4.2E-05 0.700 1.000 15 2004 2015