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rs869312961

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312961(C;G)
Make rs869312961(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position28768055
GeneFOXG1
is asnp
is mentioned by
dbSNPrs869312961
ebirs869312961
HLIrs869312961
Exacrs869312961
Varsomers869312961
Maprs869312961
PheGenIrs869312961
hapmaprs869312961
1000 genomesrs869312961
hgdprs869312961
ensemblrs869312961
gopubmedrs869312961
geneviewrs869312961
scholarrs869312961
googlers869312961
pharmgkbrs869312961
gwascentralrs869312961
openSNPrs869312961
23andMers869312961
23andMe allrs869312961
SNP Nexus

SNPshotrs869312961
SNPdbers869312961
MSV3drs869312961
GWAS Ctlgrs869312961
Max Magnitude0
ClinVar
Risk rs869312961(G;G)
Alt rs869312961(G;G)
Reference rs869312961(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene FOXG1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000014.8:g.29237261C>G
CLNSRC
CLNACC RCV000210671.1,