RS137955225 MMP21

Health Risk Chr 10:125770367 snv stop gained
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What This Variant Does
"CLNSIG=4
Associated Conditions
Visceral heterotaxy
Heterotaxy
visceral
7
autosomal
Visceral heterotaxy
Heterotaxy
visceral
7
autosomal
ClinVar Assertions (2)
NM_147191.1(MMP21):c.1203G>A (p.Trp401Ter)
· 5 submitters
NM_147191.1(MMP21):c.1203G>A (p.Trp401Ter)
· 5 submitters
Population Frequencies
gnomAD ALL
0%
1kG AFR
100%
1kG ALL
100%
1kG AMR
100%
1kG EAS
100%
1kG EUR
99.9%
1kG SAS
100%
Other Variants in MMP21
rs2493743195 rs777088158 rs747668147 rs1432707846 rs1434829861 rs773125891 rs1850488424 rs781127723 rs1487834487 rs2493742377
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