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rs2069561

From SNPedia

Orientationplus
Stabilizedplus
Make rs2069561(A;A)
Make rs2069561(A;G)
Make rs2069561(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position132963038
GeneTG
is asnp
is mentioned by
dbSNPrs2069561
ebirs2069561
HLIrs2069561
Exacrs2069561
Varsomers2069561
Maprs2069561
PheGenIrs2069561
hapmaprs2069561
1000 genomesrs2069561
hgdprs2069561
ensemblrs2069561
gopubmedrs2069561
geneviewrs2069561
scholarrs2069561
googlers2069561
pharmgkbrs2069561
gwascentralrs2069561
openSNPrs2069561
23andMers2069561
23andMe allrs2069561
SNP Nexus

SNPshotrs2069561
SNPdbers2069561
MSV3drs2069561
GWAS Ctlgrs2069561
GMAF0.3678
Max Magnitude
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene TG
allele A
frequency 0.458
sift
HuRef 1103652448242
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-D1838N
aa_change Asp1838Asn
aa_change_short D1838N
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.374326
summary