RS1057519338 AMMECR1

Health Risk Chr X:110264571
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs1057519338, also known as c.502C&gt
Associated Conditions
Midface hypoplasia
hearing impairment
elliptocytosis
and nephrocalcinosis
Midface hypoplasia
hearing impairment
elliptocytosis
and nephrocalcinosis
Other Variants in AMMECR1
rs1057519337 rs765498367 rs1569405174 rs1602891688 rs750022919 rs2148162290 rs775481785 rs2522493719 rs1453532929 rs199797010
Ask Dr. Hemsworth about this variant