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rs786204999

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204999(C;G)
Make rs786204999(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28768527
GeneFOXG1
is asnp
is mentioned by
dbSNPrs786204999
ebirs786204999
HLIrs786204999
Exacrs786204999
Varsomers786204999
Maprs786204999
PheGenIrs786204999
hapmaprs786204999
1000 genomesrs786204999
hgdprs786204999
ensemblrs786204999
gopubmedrs786204999
geneviewrs786204999
scholarrs786204999
googlers786204999
pharmgkbrs786204999
gwascentralrs786204999
openSNPrs786204999
23andMers786204999
23andMe allrs786204999
SNP Nexus

SNPshotrs786204999
SNPdbers786204999
MSV3drs786204999
GWAS Ctlgrs786204999
Max Magnitude0
ClinVar
Risk rs786204999(G;G)
Alt rs786204999(G;G)
Reference rs786204999(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29237733C>G
CLNSRC
CLNACC RCV000170070.1,