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rs267606827

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606827(A;A)
Make rs267606827(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position28768203
GeneFOXG1
is asnp
is mentioned by
dbSNPrs267606827
ebirs267606827
HLIrs267606827
Exacrs267606827
Varsomers267606827
Maprs267606827
PheGenIrs267606827
hapmaprs267606827
1000 genomesrs267606827
hgdprs267606827
ensemblrs267606827
gopubmedrs267606827
geneviewrs267606827
scholarrs267606827
googlers267606827
pharmgkbrs267606827
gwascentralrs267606827
openSNPrs267606827
23andMers267606827
23andMe allrs267606827
SNP Nexus

SNPshotrs267606827
SNPdbers267606827
MSV3drs267606827
GWAS Ctlgrs267606827
Max Magnitude0
ClinVar
Risk rs267606827(A;A)
Alt rs267606827(A;A)
Reference rs267606827(G;G)
Significance Pathogenic
Disease Rett syndrome not provided
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant not provided
Reversed 0
HGVS NC_000014.8:g.29237409G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014885.26, RCV000187469.1,