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rs148410675

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs148410675(A;G)
Make rs148410675(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28768718
GeneFOXG1
is asnp
is mentioned by
dbSNPrs148410675
ebirs148410675
HLIrs148410675
Exacrs148410675
Varsomers148410675
Maprs148410675
PheGenIrs148410675
hapmaprs148410675
1000 genomesrs148410675
hgdprs148410675
ensemblrs148410675
gopubmedrs148410675
geneviewrs148410675
scholarrs148410675
googlers148410675
pharmgkbrs148410675
gwascentralrs148410675
openSNPrs148410675
23andMers148410675
23andMe allrs148410675
SNP Nexus

SNPshotrs148410675
SNPdbers148410675
MSV3drs148410675
GWAS Ctlgrs148410675
Max Magnitude0
ClinVar
Risk rs148410675(G;G)
Alt rs148410675(G;G)
Reference rs148410675(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237924A>G
CLNSRC
CLNACC RCV000187473.2,