RS121912986 DSPP

Health Risk Chr 4:87610957
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What This Variant Does
"[OMIM:?]
Associated Conditions
Deafness
autosomal dominant nonsyndromic sensorineural 39
with dentinogenesis imperfecta 1
Deafness
autosomal dominant nonsyndromic sensorineural 39
with dentinogenesis imperfecta 1
Other Variants in DSPP
rs121912985 rs1560477489 rs121912987 rs121912989 rs1560478758 rs1560480632 rs374607352 rs61731011 rs372743728 rs201110163
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