ClinVar Miner

List of variants in gene SIX1 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
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HGVS dbSNP
NM_005982.3(SIX1):c.*1008delA rs148821608
NM_005982.3(SIX1):c.*1044G>T rs3742637
NM_005982.3(SIX1):c.*1079T>A rs559116477
NM_005982.3(SIX1):c.*1496C>T rs61993831
NM_005982.3(SIX1):c.*297T>G rs147081368
NM_005982.3(SIX1):c.*404A>G rs76116881
NM_005982.3(SIX1):c.*443A>G rs186530769
NM_005982.3(SIX1):c.*578_*581delTTTA rs556041829
NM_005982.3(SIX1):c.*602G>C rs78909843
NM_005982.3(SIX1):c.*767A>T rs574976629
NM_005982.3(SIX1):c.*890_*896delCTAGTTT rs561797428
NM_005982.3(SIX1):c.-121C>G rs375002099
NM_005982.3(SIX1):c.-137C>T rs139621918
NM_005982.3(SIX1):c.-255G>T rs79926530
NM_005982.3(SIX1):c.162G>A (p.Ala54=) rs150550985
NM_005982.3(SIX1):c.180C>G (p.Arg60=) rs781519092
NM_005982.3(SIX1):c.578A>T (p.Asn193Ile) rs142301715

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