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rs267606828

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606828(C;C)
Make rs267606828(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position28767922
GeneFOXG1
is asnp
is mentioned by
dbSNPrs267606828
ebirs267606828
HLIrs267606828
Exacrs267606828
Varsomers267606828
Maprs267606828
PheGenIrs267606828
hapmaprs267606828
1000 genomesrs267606828
hgdprs267606828
ensemblrs267606828
gopubmedrs267606828
geneviewrs267606828
scholarrs267606828
googlers267606828
pharmgkbrs267606828
gwascentralrs267606828
openSNPrs267606828
23andMers267606828
23andMe allrs267606828
SNP Nexus

SNPshotrs267606828
SNPdbers267606828
MSV3drs267606828
GWAS Ctlgrs267606828
Max Magnitude0
ClinVar
Risk rs267606828(C;C)
Alt rs267606828(C;C)
Reference rs267606828(T;T)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29237128T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014884.26,