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rs587783642

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783642(C;G)
Make rs587783642(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position28768041
GeneFOXG1
is asnp
is mentioned by
dbSNPrs587783642
ebirs587783642
HLIrs587783642
Exacrs587783642
Varsomers587783642
Maprs587783642
PheGenIrs587783642
hapmaprs587783642
1000 genomesrs587783642
hgdprs587783642
ensemblrs587783642
gopubmedrs587783642
geneviewrs587783642
scholarrs587783642
googlers587783642
pharmgkbrs587783642
gwascentralrs587783642
openSNPrs587783642
23andMers587783642
23andMe allrs587783642
SNP Nexus

SNPshotrs587783642
SNPdbers587783642
MSV3drs587783642
GWAS Ctlgrs587783642
Max Magnitude0
ClinVar
Risk rs587783642(G;G)
Alt rs587783642(G;G)
Reference rs587783642(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29237247C>G
CLNSRC
CLNACC RCV000145996.1,