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rs869320802

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869320802(C;T)
Make rs869320802(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position1213028
GeneCTBP1, CTBP1-AS
is asnp
is mentioned by
dbSNPrs869320802
ebirs869320802
HLIrs869320802
Exacrs869320802
Varsomers869320802
Maprs869320802
PheGenIrs869320802
hapmaprs869320802
1000 genomesrs869320802
hgdprs869320802
ensemblrs869320802
gopubmedrs869320802
geneviewrs869320802
scholarrs869320802
googlers869320802
pharmgkbrs869320802
gwascentralrs869320802
openSNPrs869320802
23andMers869320802
23andMe allrs869320802
SNP Nexus

SNPshotrs869320802
SNPdbers869320802
MSV3drs869320802
GWAS Ctlgrs869320802
Max Magnitude0
ClinVar
Risk rs869320802(T;T)
Alt rs869320802(T;T)
Reference rs869320802(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CTBP1-AS CTBP1
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.1206816G>A
CLNSRC
CLNACC RCV000211044.1,