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rs786205001

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205001(-;-)
Make rs786205001(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767535
GeneFOXG1
is asnp
is mentioned by
dbSNPrs786205001
ebirs786205001
HLIrs786205001
Exacrs786205001
Varsomers786205001
Maprs786205001
PheGenIrs786205001
hapmaprs786205001
1000 genomesrs786205001
hgdprs786205001
ensemblrs786205001
gopubmedrs786205001
geneviewrs786205001
scholarrs786205001
googlers786205001
pharmgkbrs786205001
gwascentralrs786205001
openSNPrs786205001
23andMers786205001
23andMe allrs786205001
SNP Nexus

SNPshotrs786205001
SNPdbers786205001
MSV3drs786205001
GWAS Ctlgrs786205001
Max Magnitude0
ClinVar
Risk rs786205001(;)
Alt rs786205001(;)
Reference rs786205001(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.29236741delC
CLNSRC
CLNACC RCV000170073.2, RCV000187475.1,