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rs879253854

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879253854(A;A)
Make rs879253854(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position123083826
GeneCLMP
is asnp
is mentioned by
dbSNPrs879253854
ebirs879253854
HLIrs879253854
Exacrs879253854
Varsomers879253854
Maprs879253854
PheGenIrs879253854
hapmaprs879253854
1000 genomesrs879253854
hgdprs879253854
ensemblrs879253854
gopubmedrs879253854
geneviewrs879253854
scholarrs879253854
googlers879253854
pharmgkbrs879253854
gwascentralrs879253854
openSNPrs879253854
23andMers879253854
23andMe allrs879253854
SNP Nexus

SNPshotrs879253854
SNPdbers879253854
MSV3drs879253854
GWAS Ctlgrs879253854
Max Magnitude0
ClinVar
Risk rs879253854(A;A)
Alt rs879253854(A;A)
Reference rs879253854(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.122954534C>T
CLNSRC
CLNACC RCV000236950.1,