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rs786205008

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205008(C;C)
Make rs786205008(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767979
GeneFOXG1
is asnp
is mentioned by
dbSNPrs786205008
ebirs786205008
HLIrs786205008
Exacrs786205008
Varsomers786205008
Maprs786205008
PheGenIrs786205008
hapmaprs786205008
1000 genomesrs786205008
hgdprs786205008
ensemblrs786205008
gopubmedrs786205008
geneviewrs786205008
scholarrs786205008
googlers786205008
pharmgkbrs786205008
gwascentralrs786205008
openSNPrs786205008
23andMers786205008
23andMe allrs786205008
SNP Nexus

SNPshotrs786205008
SNPdbers786205008
MSV3drs786205008
GWAS Ctlgrs786205008
Max Magnitude0
ClinVar
Risk rs786205008(C;C)
Alt rs786205008(C;C)
Reference rs786205008(T;T)
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.29237185T>C
CLNSRC
CLNACC RCV000170081.1, RCV000187462.1,