ClinVar Miner

List of variants in gene OAT reported as benign for cardiovascular disorder

Included ClinVar conditions (1426):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_000274.4(OAT):c.1160-59C>T rs2459217 0.91650
NM_000274.3(OAT):c.-94T>G rs4144117 0.82728
NM_000274.4(OAT):c.648+14A>G rs9422807 0.81973
NM_000274.4(OAT):c.1134C>T (p.Asn378=) rs11461 0.33660
NM_000274.4(OAT):c.199+19C>T rs10794058 0.27706
NM_000274.4(OAT):c.901-22T>C rs17619406 0.15809
NM_000274.4(OAT):c.*185C>T rs2459216 0.10300
NM_000274.4(OAT):c.*535T>C rs8182 0.06407
NM_000274.4(OAT):c.-53C>T rs117824913 0.01420
NM_000274.4(OAT):c.200-10T>C rs80313473 0.00780
NM_000274.4(OAT):c.-38C>T rs9422945 0.00489
NM_000274.4(OAT):c.969C>T (p.Tyr323=) rs138895801 0.00110
NM_000274.4(OAT):c.1224T>C (p.His408=) rs201864147 0.00073
NM_000274.4(OAT):c.1311G>T (p.Leu437Phe) rs1800456 0.00054
NM_000274.4(OAT):c.1015-6A>G rs561800688 0.00046
NM_000274.4(OAT):c.-59G>C rs144950523
NM_000274.4(OAT):c.1311G>C (p.Leu437Phe) rs1800456
NM_000274.4(OAT):c.199+11_199+16dup rs201396618
NM_000274.4(OAT):c.424+6dup rs2134477923
NM_000274.4(OAT):c.521-15_521-12del rs376636397
NM_000274.4(OAT):c.772-10del
NM_000274.4(OAT):c.772-17dup rs778743727
NM_000274.4(OAT):c.772-20del

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