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: rs10012946
rs10012946
WFS1
1 1.000 0.080 4 6291623 intron variant T/C snv 0.63 0.010 1.000 1 2008 2008