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rs138747073

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs138747073(C;T)
Make rs138747073(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position28768479
GeneFOXG1
is asnp
is mentioned by
dbSNPrs138747073
ebirs138747073
HLIrs138747073
Exacrs138747073
Varsomers138747073
Maprs138747073
PheGenIrs138747073
hapmaprs138747073
1000 genomesrs138747073
hgdprs138747073
ensemblrs138747073
gopubmedrs138747073
geneviewrs138747073
scholarrs138747073
googlers138747073
pharmgkbrs138747073
gwascentralrs138747073
openSNPrs138747073
23andMers138747073
23andMe allrs138747073
SNP Nexus

SNPshotrs138747073
SNPdbers138747073
MSV3drs138747073
GWAS Ctlgrs138747073
Max Magnitude0
ClinVar
Risk rs138747073(A,G,T;A,G,T)
Alt rs138747073(A,G,T;A,G,T)
Reference rs138747073(C;C)
Significance Pathogenic
Disease not provided Rett syndrome
Variation info
Gene FOXG1
CLNDBN not provided Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29237685C>A; NC_000014.8:g.29237685C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000170069.1, RCV000014886.26,