RS104893835 WNT7A

Health Risk Chr 3:13819120
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Schinzel phocomelia syndrome
Schinzel phocomelia syndrome
Other Variants in WNT7A
rs104893832 rs387907231 rs397514643 rs397514666 rs149962459 rs879255548 rs75651130 rs140491601 rs149363953 rs199592697
Ask Dr. Hemsworth about this variant