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rs35301433

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs35301433(A;G)
Make rs35301433(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position132871398
GeneTG
is asnp
is mentioned by
dbSNPrs35301433
ebirs35301433
HLIrs35301433
Exacrs35301433
Varsomers35301433
Maprs35301433
PheGenIrs35301433
hapmaprs35301433
1000 genomesrs35301433
hgdprs35301433
ensemblrs35301433
gopubmedrs35301433
geneviewrs35301433
scholarrs35301433
googlers35301433
pharmgkbrs35301433
gwascentralrs35301433
openSNPrs35301433
23andMers35301433
23andMe allrs35301433
SNP Nexus

SNPshotrs35301433
SNPdbers35301433
MSV3drs35301433
GWAS Ctlgrs35301433
GMAF0.001837
Max Magnitude0
Venter snp
Source plos
Gene TG
allele G
frequency
sift
HuRef 1103652448013
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.