RS2033773650 GREB1L

Health Risk Chr 18:21439536
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Associated Conditions
Profound hearing impairment
Hearing loss
autosomal dominant 80
Profound hearing impairment
Hearing loss
autosomal dominant 80
Other Variants in GREB1L
rs1555648043 rs1555661490 rs1555664772 rs1555665627 rs1555660209 rs1555662052 rs1555662061 rs1555659101 rs1555649811 rs1555661907
Ask Dr. Hemsworth about this variant