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rs587776964

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587776964(-;-)
Make rs587776964(-;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position123084670
GeneCLMP, LOC101929289
is asnp
is mentioned by
dbSNPrs587776964
ebirs587776964
HLIrs587776964
Exacrs587776964
Varsomers587776964
Maprs587776964
PheGenIrs587776964
hapmaprs587776964
1000 genomesrs587776964
hgdprs587776964
ensemblrs587776964
gopubmedrs587776964
geneviewrs587776964
scholarrs587776964
googlers587776964
pharmgkbrs587776964
gwascentralrs587776964
openSNPrs587776964
23andMers587776964
23andMe allrs587776964
SNP Nexus

SNPshotrs587776964
SNPdbers587776964
MSV3drs587776964
GWAS Ctlgrs587776964
Max Magnitude0
ClinVar
Risk rs587776964(TG,G;TG,G)
Alt rs587776964(TG,G;TG,G)
Reference rs587776964(AG;AG)
Significance Pathogenic
Disease Congenital short bowel syndrome
Variation info
Gene CLMP
CLNDBN Congenital short bowel syndrome
Reversed 1
HGVS NC_000011.9:g.122955378delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000043524.6,