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rs730880017

From SNPedia

Orientationplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs730880017(-;-)
Make rs730880017(-;CA)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position57234072
GeneTCF12
is asnp
is mentioned by
dbSNPrs730880017
ebirs730880017
HLIrs730880017
Exacrs730880017
Varsomers730880017
Maprs730880017
PheGenIrs730880017
hapmaprs730880017
1000 genomesrs730880017
hgdprs730880017
ensemblrs730880017
gopubmedrs730880017
geneviewrs730880017
scholarrs730880017
googlers730880017
pharmgkbrs730880017
gwascentralrs730880017
openSNPrs730880017
23andMers730880017
23andMe allrs730880017
SNP Nexus

SNPshotrs730880017
SNPdbers730880017
MSV3drs730880017
GWAS Ctlgrs730880017
Max Magnitude0
ClinVar
Risk rs730880017(;)
Alt rs730880017(;)
Reference rs730880017(CA;CA)
Significance Pathogenic
Disease Craniosynostosis 3
Variation info
Gene TCF12
CLNDBN Craniosynostosis 3
Reversed 0
HGVS NC_000015.9:g.57526270_57526271delCA
CLNSRC
CLNACC RCV000157614.1,