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rs121434358

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434358(A;A)
Make rs121434358(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position8605638
GeneADAMTS10
is asnp
is mentioned by
dbSNPrs121434358
ebirs121434358
HLIrs121434358
Exacrs121434358
Varsomers121434358
Maprs121434358
PheGenIrs121434358
hapmaprs121434358
1000 genomesrs121434358
hgdprs121434358
ensemblrs121434358
gopubmedrs121434358
geneviewrs121434358
scholarrs121434358
googlers121434358
pharmgkbrs121434358
gwascentralrs121434358
openSNPrs121434358
23andMers121434358
23andMe allrs121434358
SNP Nexus

SNPshotrs121434358
SNPdbers121434358
MSV3drs121434358
GWAS Ctlgrs121434358
Max Magnitude0
OMIM608990
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121434358(A;A)
Alt rs121434358(A;A)
Reference rs121434358(G;G)
Significance Pathogenic
Disease Weill-Marchesani syndrome 1
Variation info
Gene ADAMTS10
CLNDBN Weill-Marchesani syndrome 1
Reversed 1
HGVS NC_000019.9:g.8670523C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002024.3,