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rs869312700

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312700(A;A)
Make rs869312700(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position28768100
GeneFOXG1
is asnp
is mentioned by
dbSNPrs869312700
ebirs869312700
HLIrs869312700
Exacrs869312700
Varsomers869312700
Maprs869312700
PheGenIrs869312700
hapmaprs869312700
1000 genomesrs869312700
hgdprs869312700
ensemblrs869312700
gopubmedrs869312700
geneviewrs869312700
scholarrs869312700
googlers869312700
pharmgkbrs869312700
gwascentralrs869312700
openSNPrs869312700
23andMers869312700
23andMe allrs869312700
SNP Nexus

SNPshotrs869312700
SNPdbers869312700
MSV3drs869312700
GWAS Ctlgrs869312700
Max Magnitude0
ClinVar
Risk rs869312700(A;A)
Alt rs869312700(A;A)
Reference rs869312700(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29237306G>A
CLNSRC
CLNACC RCV000209877.1,