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rs11535853

From SNPedia

Merged intors2076740
Orientationplus
Stabilizedplus
Make rs11535853(C;C)
Make rs11535853(C;T)
Make rs11535853(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position132971813
GeneTG
is asnp
is mentioned by
dbSNPrs11535853
ebirs11535853
HLIrs11535853
Exacrs11535853
Varsomers11535853
Maprs11535853
PheGenIrs11535853
hapmaprs11535853
1000 genomesrs11535853
hgdprs11535853
ensemblrs11535853
gopubmedrs11535853
geneviewrs11535853
scholarrs11535853
googlers11535853
pharmgkbrs11535853
gwascentralrs11535853
openSNPrs11535853
23andMers11535853
23andMe allrs11535853
SNP Nexus

SNPshotrs11535853
SNPdbers11535853
MSV3drs11535853
GWAS Ctlgrs11535853
StatusMerged into rs2076740
Max Magnitude
? (C;C) (C;T) (T;T) 28


Venter snp
Source plos
Gene TG
allele T
frequency 0.417
sift
HuRef 1103652448295
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.