Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776966

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776966(A;A)
Make rs587776966(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position123083100
GeneCLMP, LOC101929289
is asnp
is mentioned by
dbSNPrs587776966
ebirs587776966
HLIrs587776966
Exacrs587776966
Varsomers587776966
Maprs587776966
PheGenIrs587776966
hapmaprs587776966
1000 genomesrs587776966
hgdprs587776966
ensemblrs587776966
gopubmedrs587776966
geneviewrs587776966
scholarrs587776966
googlers587776966
pharmgkbrs587776966
gwascentralrs587776966
openSNPrs587776966
23andMers587776966
23andMe allrs587776966
SNP Nexus

SNPshotrs587776966
SNPdbers587776966
MSV3drs587776966
GWAS Ctlgrs587776966
Max Magnitude0
ClinVar
Risk rs587776966(A;A)
Alt rs587776966(A;A)
Reference rs587776966(G;G)
Significance Pathogenic
Disease Congenital short bowel syndrome
Variation info
Gene CLMP
CLNDBN Congenital short bowel syndrome
Reversed 0
HGVS NC_000011.9:g.122953808G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000043526.5,