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rs587776965

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776965(C;T)
Make rs587776965(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position123074702
GeneCLMP, LOC101929289
is asnp
is mentioned by
dbSNPrs587776965
ebirs587776965
HLIrs587776965
Exacrs587776965
Varsomers587776965
Maprs587776965
PheGenIrs587776965
hapmaprs587776965
1000 genomesrs587776965
hgdprs587776965
ensemblrs587776965
gopubmedrs587776965
geneviewrs587776965
scholarrs587776965
googlers587776965
pharmgkbrs587776965
gwascentralrs587776965
openSNPrs587776965
23andMers587776965
23andMe allrs587776965
SNP Nexus

SNPshotrs587776965
SNPdbers587776965
MSV3drs587776965
GWAS Ctlgrs587776965
Max Magnitude0
ClinVar
Risk rs587776965(C,T;C,T)
Alt rs587776965(C,T;C,T)
Reference rs587776965(G;G)
Significance Pathogenic
Disease Congenital short bowel syndrome
Variation info
Gene CLMP
CLNDBN Congenital short bowel syndrome
Reversed 1
HGVS NC_000011.9:g.122945410C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043525.4,