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rs118204035

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118204035(G;T)
Make rs118204035(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position89777057
GeneMESP2
is asnp
is mentioned by
dbSNPrs118204035
ebirs118204035
HLIrs118204035
Exacrs118204035
Varsomers118204035
Maprs118204035
PheGenIrs118204035
hapmaprs118204035
1000 genomesrs118204035
hgdprs118204035
ensemblrs118204035
gopubmedrs118204035
geneviewrs118204035
scholarrs118204035
googlers118204035
pharmgkbrs118204035
gwascentralrs118204035
openSNPrs118204035
23andMers118204035
23andMe allrs118204035
SNP Nexus

SNPshotrs118204035
SNPdbers118204035
MSV3drs118204035
GWAS Ctlgrs118204035
Max Magnitude0
OMIM605195
Desc
Variant0004
Relatedalso
ClinVar
Risk rs118204035(T;T)
Alt rs118204035(T;T)
Reference rs118204035(G;G)
Significance Pathogenic
Disease Spondylocostal dysostosis 2
Variation info
Gene MESP2
CLNDBN Spondylocostal dysostosis 2
Reversed 0
HGVS NC_000015.9:g.90320288G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005495.4,