RS11570255 EDN3

Health Risk Chr 20:59300860 snv missense variant
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What This Variant Does
"[OMIM:HIRSCHSPRUNG DISEASE]
Associated Conditions
Hirschsprung disease
susceptibility to
4
Hirschsprung disease
susceptibility to
4
Population Frequencies
gnomAD ALL
99.9%
1kG AFR
100%
1kG ALL
99.6%
1kG AMR
99.9%
1kG EAS
1.8%
1kG EUR
100%
1kG SAS
0.1%
Other Variants in EDN3
rs1568823517 rs74315384 rs1568823467 rs74315385 rs267606778 rs267606779 rs369429604 rs745795470 rs977075341
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