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rs587783636

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783636(-;-)
Make rs587783636(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position28767577
GeneFOXG1
is asnp
is mentioned by
dbSNPrs587783636
ebirs587783636
HLIrs587783636
Exacrs587783636
Varsomers587783636
Maprs587783636
PheGenIrs587783636
hapmaprs587783636
1000 genomesrs587783636
hgdprs587783636
ensemblrs587783636
gopubmedrs587783636
geneviewrs587783636
scholarrs587783636
googlers587783636
pharmgkbrs587783636
gwascentralrs587783636
openSNPrs587783636
23andMers587783636
23andMe allrs587783636
SNP Nexus

SNPshotrs587783636
SNPdbers587783636
MSV3drs587783636
GWAS Ctlgrs587783636
Max Magnitude0
ClinVar
Risk rs587783636(;)
Alt rs587783636(;)
Reference rs587783636(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.29236783delC
CLNSRC
CLNACC RCV000145988.1, RCV000187476.1,