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rs587777006

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777006(A;A)
Make rs587777006(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position42249565
GeneERF
is asnp
is mentioned by
dbSNPrs587777006
ebirs587777006
HLIrs587777006
Exacrs587777006
Varsomers587777006
Maprs587777006
PheGenIrs587777006
hapmaprs587777006
1000 genomesrs587777006
hgdprs587777006
ensemblrs587777006
gopubmedrs587777006
geneviewrs587777006
scholarrs587777006
googlers587777006
pharmgkbrs587777006
gwascentralrs587777006
openSNPrs587777006
23andMers587777006
23andMe allrs587777006
SNP Nexus

SNPshotrs587777006
SNPdbers587777006
MSV3drs587777006
GWAS Ctlgrs587777006
Max Magnitude0
ClinVar
Risk rs587777006(A,G;A,G)
Alt rs587777006(A,G;A,G)
Reference rs587777006(C;C)
Significance Pathogenic
Disease Craniosynostosis 4
Variation info
Gene ERF
CLNDBN Craniosynostosis 4
Reversed 1
HGVS NC_000019.9:g.42753717G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000049336.2,