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rs2069561

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2069561(A;A)
Make rs2069561(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position132963038
GeneTG
is asnp
is mentioned by
dbSNPrs2069561
dbSNP (old)rs2069561
ClinGenrs2069561
ebirs2069561
HLIrs2069561
Exacrs2069561
Gnomadrs2069561
Varsomers2069561
Maprs2069561
PheGenIrs2069561
Biobankrs2069561
1000 genomesrs2069561
hgdprs2069561
ensemblrs2069561
gopubmedrs2069561
geneviewrs2069561
scholarrs2069561
googlers2069561
pharmgkbrs2069561
gwascentralrs2069561
openSNPrs2069561
23andMers2069561
23andMe allrs2069561
SNPshotrs2069561
SNPdbers2069561
MSV3drs2069561
GWAS Ctlgrs2069561
GMAF0.3678
Max Magnitude0
? (A;A) (A;G) (G;G) 28



ClinVar
Risk rs2069561(A;A)
Alt rs2069561(A;A)
Reference Rs2069561(G;G)
Significance Probable-non-pathogenic
Disease not specified Thyroid dyshormonogenesis
Variation info
Gene TG
CLNDBN not specified Thyroid dyshormonogenesis
Reversed 0
HGVS NC_000008.10:g.133975283G>A
CLNSRC
CLNACC RCV000242253.1, RCV000305066.1,