RS767472181 TRRAP

Health Risk Chr 7:98994846
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Associated Conditions
Hearing loss
autosomal dominant 75
Inborn genetic diseases
Hepatocellular carcinoma
Hearing loss
autosomal dominant 75
Inborn genetic diseases
Hepatocellular carcinoma
Other Variants in TRRAP
rs1562940289 rs1562945106 rs1562957569 rs1562957576 rs1584324956 rs1790093579 rs1791437854 rs1793524609 rs2116495128 rs1791432323
Ask Dr. Hemsworth about this variant