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rs879253855

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879253855(A;G)
Make rs879253855(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position123097954
GeneCLMP
is asnp
is mentioned by
dbSNPrs879253855
ebirs879253855
HLIrs879253855
Exacrs879253855
Varsomers879253855
Maprs879253855
PheGenIrs879253855
hapmaprs879253855
1000 genomesrs879253855
hgdprs879253855
ensemblrs879253855
gopubmedrs879253855
geneviewrs879253855
scholarrs879253855
googlers879253855
pharmgkbrs879253855
gwascentralrs879253855
openSNPrs879253855
23andMers879253855
23andMe allrs879253855
SNP Nexus

SNPshotrs879253855
SNPdbers879253855
MSV3drs879253855
GWAS Ctlgrs879253855
Max Magnitude0
ClinVar
Risk rs879253855(G;G)
Alt rs879253855(G;G)
Reference rs879253855(A;A)
Significance Pathogenic
Disease Congenital short bowel syndrome
Variation info
Gene CLMP
CLNDBN Congenital short bowel syndrome
Reversed 1
HGVS NC_000011.9:g.122968662T>C
CLNSRC
CLNACC RCV000236950.1,