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rs1126797

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1126797(C;T)
Make rs1126797(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position1494031
GeneTPO
is asnp
is mentioned by
dbSNPrs1126797
dbSNP (classic)rs1126797
ClinGenrs1126797
ebirs1126797
HLIrs1126797
Exacrs1126797
Gnomadrs1126797
Varsomers1126797
LitVarrs1126797
Maprs1126797
PheGenIrs1126797
Biobankrs1126797
1000 genomesrs1126797
hgdprs1126797
ensemblrs1126797
geneviewrs1126797
scholarrs1126797
googlers1126797
pharmgkbrs1126797
gwascentralrs1126797
openSNPrs1126797
23andMers1126797
SNPshotrs1126797
SNPdbers1126797
MSV3drs1126797
GWAS Ctlgrs1126797
GMAF0.376
Max Magnitude0

[PMID 24420335] Genetic analysis of thyroid peroxidase (TPO) gene in patients whose hypothyroidism was found in adulthood in West Bengal, India

ClinVar
Risk rs1126797(A;A) rs1126797(G;G) rs1126797(T;T)
Alt rs1126797(A;A) rs1126797(G;G) rs1126797(T;T)
Reference Rs1126797(C;C)
Significance Probable-non-pathogenic
Disease not specified Congenital hypothyroidism
Variation info
Gene TPO
CLNDBN not specified Congenital hypothyroidism
Reversed 0
HGVS NC_000002.11:g.1497803C>T
CLNSRC
CLNACC RCV000252817.1, RCV000358553.1,