RS2306058 ANKRD17

Health Risk Chr 4:73076960 snv synonymous variant
Upload your DNA to see your genotype for this variant.
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
Population Frequencies
gnomAD ALL
16.6%
1kG AFR
98.6%
1kG ALL
82.3%
1kG AMR
78%
1kG EAS
71.2%
1kG EUR
83.5%
1kG SAS
26.3%
Other Variants in ANKRD17
Ask Dr. Hemsworth about this variant