RS138872001 UPB1

Health Risk Chr 22:24502206 snv missense variant
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Associated Conditions
ClinVar Assertions (2)
NM_016327.3(UPB1):c.358G>T (p.Ala120Ser)
· 4 submitters
NM_016327.3(UPB1):c.358G>T (p.Ala120Ser)
· 4 submitters
Population Frequencies
gnomAD ALL
100%
1kG AFR
99.6%
1kG ALL
0.1%
1kG AMR
99.9%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in UPB1
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