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rs864621970

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864621970(A;A)
Make rs864621970(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position45431915
GeneRUNX2
is asnp
is mentioned by
dbSNPrs864621970
ebirs864621970
HLIrs864621970
Exacrs864621970
Varsomers864621970
Maprs864621970
PheGenIrs864621970
hapmaprs864621970
1000 genomesrs864621970
hgdprs864621970
ensemblrs864621970
gopubmedrs864621970
geneviewrs864621970
scholarrs864621970
googlers864621970
pharmgkbrs864621970
gwascentralrs864621970
openSNPrs864621970
23andMers864621970
23andMe allrs864621970
SNP Nexus

SNPshotrs864621970
SNPdbers864621970
MSV3drs864621970
GWAS Ctlgrs864621970
Max Magnitude0
ClinVar
Risk rs864621970(A;A)
Alt rs864621970(A;A)
Reference rs864621970(G;G)
Significance Pathogenic
Disease Cleidocranial dysostosis
Variation info
Gene RUNX2
CLNDBN Cleidocranial dysostosis
Reversed 0
HGVS NC_000006.11:g.45399652G>A
CLNSRC
CLNACC RCV000206373.1,