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: rs145518263
rs145518263
ADAM10
2 0.925 0.080 15 58665141 missense variant T/C snv 1.7E-04 1.8E-04 0.800 1.000 2 2009 2013
dbSNP: rs61751103
rs61751103
ADAM10
2 0.925 0.080 15 58665172 missense variant C/G snv 1.2E-03 1.5E-03 0.800 1.000 2 2009 2013