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: rs2238149
rs2238149
CCDC63
2 1.000 0.040 12 110874125 intron variant T/C snv 0.33 0.700 1.000 1 2010 2010