RS80358277 KCNQ4

Health Risk Chr 1:40819465
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 2A
Rare genetic deafness
KCNQ4-related disorder
Autosomal dominant nonsyndromic hearing loss 2A
Rare genetic deafness
KCNQ4-related disorder
Other Variants in KCNQ4
rs28937588 rs28939710 rs80358271 rs80358278 rs80358276 rs80358272 rs80358279 rs80358273 rs80358269 rs1648206560
Ask Dr. Hemsworth about this variant