Gene: CCDC181 ×
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: rs1208134
rs1208134
CCDC181
2 1 169459706 intron variant C/T snv 0.93 0.700 1.000 2 2011 2012
dbSNP: rs1208135
rs1208135
CCDC181
2 1 169454860 intron variant A/G;T snv 0.700 1.000 2 2011 2012