RS121912987 DSPP

Health Risk Chr 4:87612105
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What This Variant Does
"[OMIM:?]
Associated Conditions
Dentinogenesis imperfecta type 2
Dentinogenesis imperfecta type 3
Deafness
autosomal dominant nonsyndromic sensorineural 39
with dentinogenesis imperfecta 1
Monogenic hearing loss
Dentinogenesis imperfecta type 2
Dentinogenesis imperfecta type 3
Deafness
autosomal dominant nonsyndromic sensorineural 39
with dentinogenesis imperfecta 1
Monogenic hearing loss
Other Variants in DSPP
rs121912985 rs1560477489 rs121912986 rs121912989 rs1560478758 rs1560480632 rs374607352 rs61731011 rs372743728 rs201110163
Ask Dr. Hemsworth about this variant