ClinVar Miner

List of variants in gene ATP6V1B1 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (1030):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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NM_001692.4(ATP6V1B1):c.*12G>A rs77794859
NM_001692.4(ATP6V1B1):c.*68C>T rs144725809
NM_001692.4(ATP6V1B1):c.*6C>A rs45498896
NM_001692.4(ATP6V1B1):c.*80C>T rs117574187
NM_001692.4(ATP6V1B1):c.-34C>T rs79652147
NM_001692.4(ATP6V1B1):c.-89A>G rs11685700
NM_001692.4(ATP6V1B1):c.1002C>T (p.Arg334=) rs2072462
NM_001692.4(ATP6V1B1):c.1023C>T (p.Ser341=) rs117826071
NM_001692.4(ATP6V1B1):c.1248+9A>G rs78140305
NM_001692.4(ATP6V1B1):c.1320T>G (p.Ser440=) rs147250093
NM_001692.4(ATP6V1B1):c.138C>T (p.Ser46=) rs2266918
NM_001692.4(ATP6V1B1):c.1394G>A (p.Arg465His) rs142905621
NM_001692.4(ATP6V1B1):c.144C>T (p.Asn48=) rs144845223
NM_001692.4(ATP6V1B1):c.27T>C (p.Pro9=) rs17853498
NM_001692.4(ATP6V1B1):c.2T>C (p.Met1Thr) rs11681642
NM_001692.4(ATP6V1B1):c.481G>A (p.Glu161Lys) rs114234874
NM_001692.4(ATP6V1B1):c.654C>T (p.Asp218=) rs116139984
NM_001692.4(ATP6V1B1):c.89C>T (p.Thr30Ile) rs17720303

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