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rs587783641

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783641(A;G)
Make rs587783641(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position28768036
GeneFOXG1
is asnp
is mentioned by
dbSNPrs587783641
ebirs587783641
HLIrs587783641
Exacrs587783641
Varsomers587783641
Maprs587783641
PheGenIrs587783641
hapmaprs587783641
1000 genomesrs587783641
hgdprs587783641
ensemblrs587783641
gopubmedrs587783641
geneviewrs587783641
scholarrs587783641
googlers587783641
pharmgkbrs587783641
gwascentralrs587783641
openSNPrs587783641
23andMers587783641
23andMe allrs587783641
SNP Nexus

SNPshotrs587783641
SNPdbers587783641
MSV3drs587783641
GWAS Ctlgrs587783641
Max Magnitude0
ClinVar
Risk rs587783641(G;G)
Alt rs587783641(G;G)
Reference rs587783641(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29237242A>G
CLNSRC
CLNACC RCV000145995.2,