Gene: CCDC162P ×
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: rs13210693
rs13210693
CCDC162P
2 1.000 0.040 6 109277761 intron variant G/A snv 0.61 0.800 1.000 1 2011 2011