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rs796052457

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052457(A;T)
Make rs796052457(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767310
GeneFOXG1, FOXG1-AS1
is asnp
is mentioned by
dbSNPrs796052457
ebirs796052457
HLIrs796052457
Exacrs796052457
Varsomers796052457
Maprs796052457
PheGenIrs796052457
hapmaprs796052457
1000 genomesrs796052457
hgdprs796052457
ensemblrs796052457
gopubmedrs796052457
geneviewrs796052457
scholarrs796052457
googlers796052457
pharmgkbrs796052457
gwascentralrs796052457
openSNPrs796052457
23andMers796052457
23andMe allrs796052457
SNP Nexus

SNPshotrs796052457
SNPdbers796052457
MSV3drs796052457
GWAS Ctlgrs796052457
Max Magnitude0
ClinVar
Risk rs796052457(T;T)
Alt rs796052457(T;T)
Reference rs796052457(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1-AS1 FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29236516A>T
CLNSRC
CLNACC RCV000187449.1,