RS587777695 ZSWIM6

Health Risk Chr 5:61544156
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What This Variant Does
"rs587777695, also known as R1163W, is a mutation in the ZSWIM6 gene on chromosome 5. See OMIM 615951...
Associated Conditions
Acromelic frontonasal dysostosis
Inborn genetic diseases
Acromelic frontonasal dysostosis
Inborn genetic diseases
Other Variants in ZSWIM6
rs864309616 rs1554041295 rs1554041457 rs745988643 rs896504353 rs763282681 rs779283808 rs1046738327 rs943024318 rs976654292
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