RS3804100 TLR2

Health Risk Chr 4:153704256 snv missense variant

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What This Variant Does

"rs3804100, also known as 1350T/C, is a SNP in the toll-like receptor 2 TLR2 gene. A study of 700 T1D..."

Associated Conditions

TLR2-related disorder

COVID-19–associated multisystem inflammatory syndrome in adults

TLR2-related disorder

COVID-19–associated multisystem inflammatory syndrome in adults

GWAS Studies (1)

Trait	Risk Allele	OR / Beta	P-value	Study
Height	C	β: 0.006	3E-7	PubMed

Population Frequencies

gnomAD ALL

8.2%

1kG AFR

4.9%

1kG ALL

10.8%

1kG AMR

94.4%

1kG EAS

76.1%

1kG EUR

6.4%

1kG SAS

13.7%

Other Variants in TLR2