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rs267606736

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606736(C;T)
Make rs267606736(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position100205167
GeneCHUK
is asnp
is mentioned by
dbSNPrs267606736
ebirs267606736
HLIrs267606736
Exacrs267606736
Varsomers267606736
Maprs267606736
PheGenIrs267606736
hapmaprs267606736
1000 genomesrs267606736
hgdprs267606736
ensemblrs267606736
gopubmedrs267606736
geneviewrs267606736
scholarrs267606736
googlers267606736
pharmgkbrs267606736
gwascentralrs267606736
openSNPrs267606736
23andMers267606736
23andMe allrs267606736
SNP Nexus

SNPshotrs267606736
SNPdbers267606736
MSV3drs267606736
GWAS Ctlgrs267606736
Max Magnitude0
ClinVar
Risk rs267606736(T;T)
Alt rs267606736(T;T)
Reference rs267606736(C;C)
Significance Pathogenic
Disease Cocoon syndrome
Variation info
Gene CHUK
CLNDBN Cocoon syndrome
Reversed 1
HGVS NC_000010.10:g.101964924G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009502.2,