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rs113994156

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs113994156(A;G)
Make rs113994156(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position89776628
GeneMESP2
is asnp
is mentioned by
dbSNPrs113994156
ebirs113994156
HLIrs113994156
Exacrs113994156
Varsomers113994156
Maprs113994156
PheGenIrs113994156
hapmaprs113994156
1000 genomesrs113994156
hgdprs113994156
ensemblrs113994156
gopubmedrs113994156
geneviewrs113994156
scholarrs113994156
googlers113994156
pharmgkbrs113994156
gwascentralrs113994156
openSNPrs113994156
23andMers113994156
23andMe allrs113994156
SNP Nexus

SNPshotrs113994156
SNPdbers113994156
MSV3drs113994156
GWAS Ctlgrs113994156
Max Magnitude0
ClinVar
Risk rs113994156(G;G)
Alt rs113994156(G;G)
Reference rs113994156(A;A)
Significance Pathogenic
Disease Spondylocostal dysostosis 2
Variation info
Gene MESP2
CLNDBN Spondylocostal dysostosis 2
Reversed 0
HGVS NC_000015.9:g.90319859A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000032156.1,