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rs864321681

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864321681(A;G)
Make rs864321681(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position42254999
GeneERF
is asnp
is mentioned by
dbSNPrs864321681
ebirs864321681
HLIrs864321681
Exacrs864321681
Varsomers864321681
Maprs864321681
PheGenIrs864321681
hapmaprs864321681
1000 genomesrs864321681
hgdprs864321681
ensemblrs864321681
gopubmedrs864321681
geneviewrs864321681
scholarrs864321681
googlers864321681
pharmgkbrs864321681
gwascentralrs864321681
openSNPrs864321681
23andMers864321681
23andMe allrs864321681
SNP Nexus

SNPshotrs864321681
SNPdbers864321681
MSV3drs864321681
GWAS Ctlgrs864321681
Max Magnitude0
ClinVar
Risk rs864321681(G;G)
Alt rs864321681(G;G)
Reference rs864321681(A;A)
Significance Pathogenic
Disease Craniosynostosis 4
Variation info
Gene ERF
CLNDBN Craniosynostosis 4
Reversed 1
HGVS NC_000019.9:g.42759151T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000203306.2,