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rs367624766

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs367624766(A;A)
Make rs367624766(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position214640082
GeneCENPF
is asnp
is mentioned by
dbSNPrs367624766
ebirs367624766
HLIrs367624766
Exacrs367624766
Varsomers367624766
Maprs367624766
PheGenIrs367624766
hapmaprs367624766
1000 genomesrs367624766
hgdprs367624766
ensemblrs367624766
gopubmedrs367624766
geneviewrs367624766
scholarrs367624766
googlers367624766
pharmgkbrs367624766
gwascentralrs367624766
openSNPrs367624766
23andMers367624766
23andMe allrs367624766
SNP Nexus

SNPshotrs367624766
SNPdbers367624766
MSV3drs367624766
GWAS Ctlgrs367624766
Max Magnitude0
ClinVar
Risk rs367624766(A,T;A,T)
Alt rs367624766(A,T;A,T)
Reference rs367624766(G;G)
Significance Pathogenic
Disease Stromme syndrome
Variation info
Gene CENPF
CLNDBN Stromme syndrome
Reversed 0
HGVS NC_000001.10:g.214813425G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000170523.3,