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rs2069556

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 0
Make rs2069556(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position132908273
GeneTG
is asnp
is mentioned by
dbSNPrs2069556
dbSNP (classic)rs2069556
ClinGenrs2069556
ebirs2069556
HLIrs2069556
Exacrs2069556
Gnomadrs2069556
Varsomers2069556
LitVarrs2069556
Maprs2069556
PheGenIrs2069556
Biobankrs2069556
1000 genomesrs2069556
hgdprs2069556
ensemblrs2069556
geneviewrs2069556
scholarrs2069556
googlers2069556
pharmgkbrs2069556
gwascentralrs2069556
openSNPrs2069556
23andMers2069556
SNPshotrs2069556
SNPdbers2069556
MSV3drs2069556
GWAS Ctlgrs2069556
GMAF0.4215
Max Magnitude0
? (A;A) (A;G) (G;G) 28





ClinVar
Risk rs2069556(G;G)
Alt rs2069556(G;G)
Reference Rs2069556(A;A)
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.133920518A>G
CLNSRC
CLNACC RCV000241944.1, RCV000280505.1,



[PMID 28345837OA-icon.png] Association of the Asp1312Gly Thyroglobulin Gene Polymorphism with Susceptibility to Differentiated Thyroid Cancer in an Iranian Population