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rs765907815

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs765907815(A;A)
Make rs765907815(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position123083728
GeneCLMP, LOC101929289
is asnp
is mentioned by
dbSNPrs765907815
ebirs765907815
HLIrs765907815
Exacrs765907815
Varsomers765907815
Maprs765907815
PheGenIrs765907815
hapmaprs765907815
1000 genomesrs765907815
hgdprs765907815
ensemblrs765907815
gopubmedrs765907815
geneviewrs765907815
scholarrs765907815
googlers765907815
pharmgkbrs765907815
gwascentralrs765907815
openSNPrs765907815
23andMers765907815
23andMe allrs765907815
SNP Nexus

SNPshotrs765907815
SNPdbers765907815
MSV3drs765907815
GWAS Ctlgrs765907815
Max Magnitude0
ClinVar
Risk rs765907815(A;A)
Alt rs765907815(A;A)
Reference rs765907815(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.122954436G>A
CLNSRC
CLNACC RCV000236558.1,