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rs730880016

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880016(A;A)
Make rs730880016(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position57273122
GeneTCF12
is asnp
is mentioned by
dbSNPrs730880016
ebirs730880016
HLIrs730880016
Exacrs730880016
Varsomers730880016
Maprs730880016
PheGenIrs730880016
hapmaprs730880016
1000 genomesrs730880016
hgdprs730880016
ensemblrs730880016
gopubmedrs730880016
geneviewrs730880016
scholarrs730880016
googlers730880016
pharmgkbrs730880016
gwascentralrs730880016
openSNPrs730880016
23andMers730880016
23andMe allrs730880016
SNP Nexus

SNPshotrs730880016
SNPdbers730880016
MSV3drs730880016
GWAS Ctlgrs730880016
Max Magnitude0
ClinVar
Risk rs730880016(A;A)
Alt rs730880016(A;A)
Reference rs730880016(G;G)
Significance Pathogenic
Disease Craniosynostosis 3
Variation info
Gene TCF12
CLNDBN Craniosynostosis 3
Reversed 0
HGVS NC_000015.9:g.57565320G>A
CLNSRC
CLNACC RCV000157617.1,