RS786203989 PAM16

Health Risk Chr 16:4340985
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive spondylometaphyseal dysplasia
Megarbane type
Autosomal recessive spondylometaphyseal dysplasia
Megarbane type
Other Variants in PAM16
rs1596247721
Ask Dr. Hemsworth about this variant