Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205004

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205004(-;-)
Make rs786205004(-;C)
Make rs786205004(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767831
GeneFOXG1
is asnp
is mentioned by
dbSNPrs786205004
ebirs786205004
HLIrs786205004
Exacrs786205004
Varsomers786205004
Maprs786205004
PheGenIrs786205004
hapmaprs786205004
1000 genomesrs786205004
hgdprs786205004
ensemblrs786205004
gopubmedrs786205004
geneviewrs786205004
scholarrs786205004
googlers786205004
pharmgkbrs786205004
gwascentralrs786205004
openSNPrs786205004
23andMers786205004
23andMe allrs786205004
SNP Nexus

SNPshotrs786205004
SNPdbers786205004
MSV3drs786205004
GWAS Ctlgrs786205004
Max Magnitude0
ClinVar
Risk rs786205004(C;C)
Alt rs786205004(C;C)
Reference rs786205004(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29237037dupC
CLNSRC
CLNACC RCV000170077.1,