RS767387863 DSPP

Health Risk Chr 4:87613217
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Associated Conditions
Deafness
autosomal dominant 39
with dentinogenesis imperfecta 1
Inborn genetic diseases
Deafness
autosomal dominant 39
with dentinogenesis imperfecta 1
Inborn genetic diseases
Other Variants in DSPP
rs121912985 rs1560477489 rs121912986 rs121912987 rs121912989 rs1560478758 rs1560480632 rs374607352 rs61731011 rs372743728
Ask Dr. Hemsworth about this variant