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rs587777009

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777009(C;T)
Make rs587777009(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position42250394
GeneERF
is asnp
is mentioned by
dbSNPrs587777009
ebirs587777009
HLIrs587777009
Exacrs587777009
Varsomers587777009
Maprs587777009
PheGenIrs587777009
hapmaprs587777009
1000 genomesrs587777009
hgdprs587777009
ensemblrs587777009
gopubmedrs587777009
geneviewrs587777009
scholarrs587777009
googlers587777009
pharmgkbrs587777009
gwascentralrs587777009
openSNPrs587777009
23andMers587777009
23andMe allrs587777009
SNP Nexus

SNPshotrs587777009
SNPdbers587777009
MSV3drs587777009
GWAS Ctlgrs587777009
Max Magnitude0
ClinVar
Risk rs587777009(C,T;C,T)
Alt rs587777009(C,T;C,T)
Reference rs587777009(G;G)
Significance Pathogenic
Disease Craniosynostosis 4
Variation info
Gene ERF
CLNDBN Craniosynostosis 4
Reversed 1
HGVS NC_000019.9:g.42754546C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000049339.2,