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rs587777010

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777010(A;A)
Make rs587777010(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position42248842
GeneERF
is asnp
is mentioned by
dbSNPrs587777010
ebirs587777010
HLIrs587777010
Exacrs587777010
Varsomers587777010
Maprs587777010
PheGenIrs587777010
hapmaprs587777010
1000 genomesrs587777010
hgdprs587777010
ensemblrs587777010
gopubmedrs587777010
geneviewrs587777010
scholarrs587777010
googlers587777010
pharmgkbrs587777010
gwascentralrs587777010
openSNPrs587777010
23andMers587777010
23andMe allrs587777010
SNP Nexus

SNPshotrs587777010
SNPdbers587777010
MSV3drs587777010
GWAS Ctlgrs587777010
Max Magnitude0
ClinVar
Risk rs587777010(A,G;A,G)
Alt rs587777010(A,G;A,G)
Reference rs587777010(C;C)
Significance Pathogenic
Disease Craniosynostosis 4
Variation info
Gene ERF
CLNDBN Craniosynostosis 4
Reversed 1
HGVS NC_000019.9:g.42752994G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000049340.2,