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rs397515538

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515538(-;-)
Make rs397515538(-;C)
Make rs397515538(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position45422624
GeneRUNX2
is asnp
is mentioned by
dbSNPrs397515538
ebirs397515538
HLIrs397515538
Exacrs397515538
Varsomers397515538
Maprs397515538
PheGenIrs397515538
hapmaprs397515538
1000 genomesrs397515538
hgdprs397515538
ensemblrs397515538
gopubmedrs397515538
geneviewrs397515538
scholarrs397515538
googlers397515538
pharmgkbrs397515538
gwascentralrs397515538
openSNPrs397515538
23andMers397515538
23andMe allrs397515538
SNP Nexus

SNPshotrs397515538
SNPdbers397515538
MSV3drs397515538
GWAS Ctlgrs397515538
Max Magnitude0
ClinVar
Risk rs397515538(C;C)
Alt rs397515538(C;C)
Reference rs397515538(;)
Significance Pathogenic
Disease Cleidocranial dysostosis
Variation info
Gene RUNX2
CLNDBN Cleidocranial dysostosis
Reversed 0
HGVS NC_000006.11:g.45390361dupC
CLNSRC ClinVar GeneReviews
CLNACC RCV000055837.1,