RS201387261 SPTBN4

Health Risk Chr 19:40556098
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Associated Conditions
Inborn genetic diseases
Neurodevelopmental disorder with hypotonia
neuropathy
and deafness
Inborn genetic diseases
Neurodevelopmental disorder with hypotonia
neuropathy
and deafness
Other Variants in SPTBN4
rs1114167445 rs1555815437 rs1555818396 rs777273785 rs1555721549 rs1599794560 rs1599759068 rs1599819198 rs2080330778 rs2080555011
Ask Dr. Hemsworth about this variant