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rs730880015

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880015(-;-)
Make rs730880015(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position57243507
GeneTCF12
is asnp
is mentioned by
dbSNPrs730880015
ebirs730880015
HLIrs730880015
Exacrs730880015
Varsomers730880015
Maprs730880015
PheGenIrs730880015
hapmaprs730880015
1000 genomesrs730880015
hgdprs730880015
ensemblrs730880015
gopubmedrs730880015
geneviewrs730880015
scholarrs730880015
googlers730880015
pharmgkbrs730880015
gwascentralrs730880015
openSNPrs730880015
23andMers730880015
23andMe allrs730880015
SNP Nexus

SNPshotrs730880015
SNPdbers730880015
MSV3drs730880015
GWAS Ctlgrs730880015
Max Magnitude0
ClinVar
Risk rs730880015(;)
Alt rs730880015(;)
Reference rs730880015(G;G)
Significance Pathogenic
Disease Craniosynostosis 3
Variation info
Gene TCF12
CLNDBN Craniosynostosis 3
Reversed 0
HGVS NC_000015.9:g.57535705delG
CLNSRC
CLNACC RCV000157615.1,