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rs118204034

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118204034(G;T)
Make rs118204034(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position89776598
GeneMESP2
is asnp
is mentioned by
dbSNPrs118204034
ebirs118204034
HLIrs118204034
Exacrs118204034
Varsomers118204034
Maprs118204034
PheGenIrs118204034
hapmaprs118204034
1000 genomesrs118204034
hgdprs118204034
ensemblrs118204034
gopubmedrs118204034
geneviewrs118204034
scholarrs118204034
googlers118204034
pharmgkbrs118204034
gwascentralrs118204034
openSNPrs118204034
23andMers118204034
23andMe allrs118204034
SNP Nexus

SNPshotrs118204034
SNPdbers118204034
MSV3drs118204034
GWAS Ctlgrs118204034
Max Magnitude0
ClinVar
Risk rs118204034(T;T)
Alt rs118204034(T;T)
Reference rs118204034(G;G)
Significance Pathogenic
Disease Spondylocostal dysostosis 2
Variation info
Gene MESP2
CLNDBN Spondylocostal dysostosis 2
Reversed 0
HGVS NC_000015.9:g.90319829G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000032155.1,