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

rs786205005

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205005(A;A)
Make rs786205005(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767856
GeneFOXG1
is asnp
is mentioned by
dbSNPrs786205005
ebirs786205005
HLIrs786205005
Exacrs786205005
Varsomers786205005
Maprs786205005
PheGenIrs786205005
hapmaprs786205005
1000 genomesrs786205005
hgdprs786205005
ensemblrs786205005
gopubmedrs786205005
geneviewrs786205005
scholarrs786205005
googlers786205005
pharmgkbrs786205005
gwascentralrs786205005
openSNPrs786205005
23andMers786205005
23andMe allrs786205005
SNP Nexus

SNPshotrs786205005
SNPdbers786205005
MSV3drs786205005
GWAS Ctlgrs786205005
Max Magnitude0
ClinVar
Risk rs786205005(A;A)
Alt rs786205005(A;A)
Reference rs786205005(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29237062G>A
CLNSRC
CLNACC RCV000170078.1,