RS11130760 FHIT

Health Risk Chr 3:60210808 snv intron variant

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What This Variant Does

"Multiple single nucleotide polymorphism analysis and association of specific genotypes in FHIT, SAMD4A, and ANKRD17 in Indian patients with oral cancer."

Associated Conditions

Lip and oral cavity carcinoma

Population Frequencies

1kG AFR

12.5%

1kG ALL

12.3%

1kG AMR

9.4%

1kG EAS

12.3%

1kG EUR

10.1%

1kG SAS

83.4%

Ask Dr. Hemsworth about this variant