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rs267606636

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606636(A;A)
Make rs267606636(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position8592797
GeneADAMTS10
is asnp
is mentioned by
dbSNPrs267606636
ebirs267606636
HLIrs267606636
Exacrs267606636
Varsomers267606636
Maprs267606636
PheGenIrs267606636
hapmaprs267606636
1000 genomesrs267606636
hgdprs267606636
ensemblrs267606636
gopubmedrs267606636
geneviewrs267606636
scholarrs267606636
googlers267606636
pharmgkbrs267606636
gwascentralrs267606636
openSNPrs267606636
23andMers267606636
23andMe allrs267606636
SNP Nexus

SNPshotrs267606636
SNPdbers267606636
MSV3drs267606636
GWAS Ctlgrs267606636
Max Magnitude0
ClinVar
Risk rs267606636(A;A)
Alt rs267606636(A;A)
Reference rs267606636(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.8657681C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002026.3,