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rs587777008

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777008(A;A)
Make rs587777008(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position42250332
GeneERF
is asnp
is mentioned by
dbSNPrs587777008
ebirs587777008
HLIrs587777008
Exacrs587777008
Varsomers587777008
Maprs587777008
PheGenIrs587777008
hapmaprs587777008
1000 genomesrs587777008
hgdprs587777008
ensemblrs587777008
gopubmedrs587777008
geneviewrs587777008
scholarrs587777008
googlers587777008
pharmgkbrs587777008
gwascentralrs587777008
openSNPrs587777008
23andMers587777008
23andMe allrs587777008
SNP Nexus

SNPshotrs587777008
SNPdbers587777008
MSV3drs587777008
GWAS Ctlgrs587777008
Max Magnitude0
ClinVar
Risk rs587777008(A,G;A,G)
Alt rs587777008(A,G;A,G)
Reference rs587777008(C;C)
Significance Pathogenic
Disease Craniosynostosis 4
Variation info
Gene ERF
CLNDBN Craniosynostosis 4
Reversed 1
HGVS NC_000019.9:g.42754484G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000049338.2,