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rs869312717

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312717(-;-)
Make rs869312717(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position28767733
GeneFOXG1
is asnp
is mentioned by
dbSNPrs869312717
ClinGenrs869312717
ebirs869312717
HLIrs869312717
Exacrs869312717
Varsomers869312717
Maprs869312717
PheGenIrs869312717
hapmaprs869312717
1000 genomesrs869312717
hgdprs869312717
ensemblrs869312717
gopubmedrs869312717
geneviewrs869312717
scholarrs869312717
googlers869312717
pharmgkbrs869312717
gwascentralrs869312717
openSNPrs869312717
23andMers869312717
23andMe allrs869312717
SNP Nexus

SNPshotrs869312717
SNPdbers869312717
MSV3drs869312717
GWAS Ctlgrs869312717
Max Magnitude0
ClinVar
Risk rs869312717(-;-)
Alt rs869312717(-;-)
Reference Rs869312717(G;G)
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.29236945delG
CLNSRC
CLNACC RCV000209851.1, RCV000414502.1,