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rs2069556

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 0
Make rs2069556(A;A)
Make rs2069556(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position132908273
GeneTG
is asnp
is mentioned by
dbSNPrs2069556
ebirs2069556
HLIrs2069556
Exacrs2069556
Varsomers2069556
Maprs2069556
PheGenIrs2069556
hapmaprs2069556
1000 genomesrs2069556
hgdprs2069556
ensemblrs2069556
gopubmedrs2069556
geneviewrs2069556
scholarrs2069556
googlers2069556
pharmgkbrs2069556
gwascentralrs2069556
openSNPrs2069556
23andMers2069556
23andMe allrs2069556
SNP Nexus

SNPshotrs2069556
SNPdbers2069556
MSV3drs2069556
GWAS Ctlgrs2069556
GMAF0.4215
Max Magnitude0
? (A;A) (A;G) (G;G) 28


Venter snp
Source plos
Gene TG
allele G
frequency 0.558
sift TOLERATED
HuRef 1103652448081
Disease Association Defects in TG are a cause of some forms of goiter (MIM:188450). Goiter is an enlargement of the thyroid gland. This is sometimes linked to hypothyroidism.



GET Evidence
TG-D1312G
aa_change Asp1312Gly
aa_change_short D1312G
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.455754
summary