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rs587783643

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783643(A;A)
Make rs587783643(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position28768078
GeneFOXG1
is asnp
is mentioned by
dbSNPrs587783643
ebirs587783643
HLIrs587783643
Exacrs587783643
Varsomers587783643
Maprs587783643
PheGenIrs587783643
hapmaprs587783643
1000 genomesrs587783643
hgdprs587783643
ensemblrs587783643
gopubmedrs587783643
geneviewrs587783643
scholarrs587783643
googlers587783643
pharmgkbrs587783643
gwascentralrs587783643
openSNPrs587783643
23andMers587783643
23andMe allrs587783643
SNP Nexus

SNPshotrs587783643
SNPdbers587783643
MSV3drs587783643
GWAS Ctlgrs587783643
Max Magnitude0
ClinVar
Risk rs587783643(A;A)
Alt rs587783643(A;A)
Reference rs587783643(G;G)
Significance Probable-Pathogenic
Disease Rett syndrome
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29237284G>A
CLNSRC
CLNACC RCV000145998.1,