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rs864321680

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864321680(A;G)
Make rs864321680(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position42250567
GeneERF
is asnp
is mentioned by
dbSNPrs864321680
ebirs864321680
HLIrs864321680
Exacrs864321680
Varsomers864321680
Maprs864321680
PheGenIrs864321680
hapmaprs864321680
1000 genomesrs864321680
hgdprs864321680
ensemblrs864321680
gopubmedrs864321680
geneviewrs864321680
scholarrs864321680
googlers864321680
pharmgkbrs864321680
gwascentralrs864321680
openSNPrs864321680
23andMers864321680
23andMe allrs864321680
SNP Nexus

SNPshotrs864321680
SNPdbers864321680
MSV3drs864321680
GWAS Ctlgrs864321680
Max Magnitude0
ClinVar
Risk rs864321680(G;G)
Alt rs864321680(G;G)
Reference rs864321680(A;A)
Significance Pathogenic
Disease Craniosynostosis 4
Variation info
Gene ERF
CLNDBN Craniosynostosis 4
Reversed 1
HGVS NC_000019.9:g.42754719T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000203301.2,