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rs398124202

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124202(A;A)
Make rs398124202(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position28767535
GeneFOXG1
is asnp
is mentioned by
dbSNPrs398124202
ebirs398124202
HLIrs398124202
Exacrs398124202
Varsomers398124202
Maprs398124202
PheGenIrs398124202
hapmaprs398124202
1000 genomesrs398124202
hgdprs398124202
ensemblrs398124202
gopubmedrs398124202
geneviewrs398124202
scholarrs398124202
googlers398124202
pharmgkbrs398124202
gwascentralrs398124202
openSNPrs398124202
23andMers398124202
23andMe allrs398124202
SNP Nexus

SNPshotrs398124202
SNPdbers398124202
MSV3drs398124202
GWAS Ctlgrs398124202
Max Magnitude0
ClinVar
Risk rs398124202(A,T;A,T)
Alt rs398124202(A,T;A,T)
Reference rs398124202(C;C)
Significance Pathogenic
Disease not provided Rett syndrome
Variation info
Gene FOXG1
CLNDBN not provided Rett syndrome, congenital variant
Reversed 0
HGVS NC_000014.8:g.29236741C>A; NC_000014.8:g.29236741C>T
CLNSRC
CLNACC RCV000081279.4, RCV000170072.1, RCV000187451.2,