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: rs104894738
rs104894738
AMELX ; ARHGAP6
3 0.882 0.080 X 11294799 missense variant G/C snv 0.010 1.000 1 2004 2004