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rs587783640

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783640(G;T)
Make rs587783640(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position28768034
GeneFOXG1
is asnp
is mentioned by
dbSNPrs587783640
ebirs587783640
HLIrs587783640
Exacrs587783640
Varsomers587783640
Maprs587783640
PheGenIrs587783640
hapmaprs587783640
1000 genomesrs587783640
hgdprs587783640
ensemblrs587783640
gopubmedrs587783640
geneviewrs587783640
scholarrs587783640
googlers587783640
pharmgkbrs587783640
gwascentralrs587783640
openSNPrs587783640
23andMers587783640
23andMe allrs587783640
SNP Nexus

SNPshotrs587783640
SNPdbers587783640
MSV3drs587783640
GWAS Ctlgrs587783640
Max Magnitude0
ClinVar
Risk rs587783640(T;T)
Alt rs587783640(T;T)
Reference rs587783640(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.29237240G>T
CLNSRC
CLNACC RCV000145994.1, RCV000170083.1,