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rs879255530

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879255530(A;T)
Make rs879255530(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position28767832
GeneFOXG1
is asnp
is mentioned by
dbSNPrs879255530
ebirs879255530
HLIrs879255530
Exacrs879255530
Varsomers879255530
Maprs879255530
PheGenIrs879255530
hapmaprs879255530
1000 genomesrs879255530
hgdprs879255530
ensemblrs879255530
gopubmedrs879255530
geneviewrs879255530
scholarrs879255530
googlers879255530
pharmgkbrs879255530
gwascentralrs879255530
openSNPrs879255530
23andMers879255530
23andMe allrs879255530
SNP Nexus

SNPshotrs879255530
SNPdbers879255530
MSV3drs879255530
GWAS Ctlgrs879255530
Max Magnitude0
ClinVar
Risk rs879255530(T;T)
Alt rs879255530(T;T)
Reference rs879255530(A;A)
Significance Probable-Pathogenic
Disease Rett syndrome
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29237038A>T
CLNSRC
CLNACC RCV000239423.1,