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rs387906266

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906266(A;A)
Make rs387906266(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position8600927
GeneADAMTS10
is asnp
is mentioned by
dbSNPrs387906266
ebirs387906266
HLIrs387906266
Exacrs387906266
Varsomers387906266
Maprs387906266
PheGenIrs387906266
hapmaprs387906266
1000 genomesrs387906266
hgdprs387906266
ensemblrs387906266
gopubmedrs387906266
geneviewrs387906266
scholarrs387906266
googlers387906266
pharmgkbrs387906266
gwascentralrs387906266
openSNPrs387906266
23andMers387906266
23andMe allrs387906266
SNP Nexus

SNPshotrs387906266
SNPdbers387906266
MSV3drs387906266
GWAS Ctlgrs387906266
Max Magnitude0
ClinVar
Risk rs387906266(A;A)
Alt rs387906266(A;A)
Reference rs387906266(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.8665811C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002023.3,