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rs587783638

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783638(C;G)
Make rs587783638(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position28767842
GeneFOXG1
is asnp
is mentioned by
dbSNPrs587783638
ebirs587783638
HLIrs587783638
Exacrs587783638
Varsomers587783638
Maprs587783638
PheGenIrs587783638
hapmaprs587783638
1000 genomesrs587783638
hgdprs587783638
ensemblrs587783638
gopubmedrs587783638
geneviewrs587783638
scholarrs587783638
googlers587783638
pharmgkbrs587783638
gwascentralrs587783638
openSNPrs587783638
23andMers587783638
23andMe allrs587783638
SNP Nexus

SNPshotrs587783638
SNPdbers587783638
MSV3drs587783638
GWAS Ctlgrs587783638
Max Magnitude0
ClinVar
Risk rs587783638(G;G)
Alt rs587783638(G;G)
Reference rs587783638(C;C)
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.29237048C>G
CLNSRC
CLNACC RCV000145992.1, RCV000170068.1,