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rs267606826

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606826(C;G)
Make rs267606826(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position28767903
GeneFOXG1
is asnp
is mentioned by
dbSNPrs267606826
ebirs267606826
HLIrs267606826
Exacrs267606826
Varsomers267606826
Maprs267606826
PheGenIrs267606826
hapmaprs267606826
1000 genomesrs267606826
hgdprs267606826
ensemblrs267606826
gopubmedrs267606826
geneviewrs267606826
scholarrs267606826
googlers267606826
pharmgkbrs267606826
gwascentralrs267606826
openSNPrs267606826
23andMers267606826
23andMe allrs267606826
SNP Nexus

SNPshotrs267606826
SNPdbers267606826
MSV3drs267606826
GWAS Ctlgrs267606826
Max Magnitude0
ClinVar
Risk rs267606826(G,T;G,T)
Alt rs267606826(G,T;G,T)
Reference rs267606826(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29237109C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014883.25,