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rs2292305

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2292305(C;C)
Make rs2292305(C;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position39588621
GeneTHBS1
is asnp
is mentioned by
dbSNPrs2292305
dbSNP (classic)rs2292305
ClinGenrs2292305
ebirs2292305
HLIrs2292305
Exacrs2292305
Gnomadrs2292305
Varsomers2292305
LitVarrs2292305
Maprs2292305
PheGenIrs2292305
Biobankrs2292305
1000 genomesrs2292305
hgdprs2292305
ensemblrs2292305
geneviewrs2292305
scholarrs2292305
googlers2292305
pharmgkbrs2292305
gwascentralrs2292305
openSNPrs2292305
23andMers2292305
SNPshotrs2292305
SNPdbers2292305
MSV3drs2292305
GWAS Ctlgrs2292305
GMAF0.2534
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 22011138] Polymorphism of THBS1 rs1478604 A>G in 5-Untranslated Region Is Associated with Lymph Node Metastasis of Gastric Cancer in a Southeast Chinese Population

[PMID 18454203OA-icon.png] Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.

[PMID 18787196OA-icon.png] Segment-specific genetic effects on carotid intima-media thickness: the Northern Manhattan study.

[PMID 22311024] Association of thrombospondin 1 gene with schizophrenia in Korean population.



ClinVar
Risk rs2292305(C;C) rs2292305(G;G)
Alt rs2292305(C;C) rs2292305(G;G)
Reference Rs2292305(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene THBS1
CLNDBN not specified
Reversed 1
HGVS NC_000015.9:g.39880822A>G
CLNSRC
CLNACC RCV000455296.1,