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rs267606637

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606637(A;A)
Make rs267606637(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position8589302
GeneADAMTS10
is asnp
is mentioned by
dbSNPrs267606637
ebirs267606637
HLIrs267606637
Exacrs267606637
Varsomers267606637
Maprs267606637
PheGenIrs267606637
hapmaprs267606637
1000 genomesrs267606637
hgdprs267606637
ensemblrs267606637
gopubmedrs267606637
geneviewrs267606637
scholarrs267606637
googlers267606637
pharmgkbrs267606637
gwascentralrs267606637
openSNPrs267606637
23andMers267606637
23andMe allrs267606637
SNP Nexus

SNPshotrs267606637
SNPdbers267606637
MSV3drs267606637
GWAS Ctlgrs267606637
Max Magnitude0
ClinVar
Risk rs267606637(A,T;A,T)
Alt rs267606637(A,T;A,T)
Reference rs267606637(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.8654186C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002027.3,