RS104893922 SMN1

Health Risk Chr 5:70946157
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What This Variant Does
"rs104893922, also known as c.815A&gt
Associated Conditions
Werdnig-Hoffmann disease
Spinal muscular atrophy
Werdnig-Hoffmann disease
Spinal muscular atrophy
Other Variants in SMN1
rs1554066666 rs1554066659 rs76163360 rs1554066397 rs2112814388 rs75991011 rs104893931 rs77804083 rs104893930 rs104893927
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