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rs398122381

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122381(C;G)
Make rs398122381(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position57232327
GeneTCF12
is asnp
is mentioned by
dbSNPrs398122381
ebirs398122381
HLIrs398122381
Exacrs398122381
Varsomers398122381
Maprs398122381
PheGenIrs398122381
hapmaprs398122381
1000 genomesrs398122381
hgdprs398122381
ensemblrs398122381
gopubmedrs398122381
geneviewrs398122381
scholarrs398122381
googlers398122381
pharmgkbrs398122381
gwascentralrs398122381
openSNPrs398122381
23andMers398122381
23andMe allrs398122381
SNP Nexus

SNPshotrs398122381
SNPdbers398122381
MSV3drs398122381
GWAS Ctlgrs398122381
Max Magnitude0
ClinVar
Risk rs398122381(G;G)
Alt rs398122381(G;G)
Reference rs398122381(C;C)
Significance Pathogenic
Disease Craniosynostosis 3
Variation info
Gene TCF12
CLNDBN Craniosynostosis 3
Reversed 0
HGVS NC_000015.9:g.57524525C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000049326.4,