ClinVar Miner

List of variants in gene SIX1 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_005982.4(SIX1):c.*1001T>C rs886050568
NM_005982.4(SIX1):c.*1268_*1269AT[1] rs3832952
NM_005982.4(SIX1):c.*1571T>C rs886050567
NM_005982.4(SIX1):c.*161C>A rs886050571
NM_005982.4(SIX1):c.*268_*271CAAA[2] rs886050570
NM_005982.4(SIX1):c.*371A>G rs538935374
NM_005982.4(SIX1):c.*736T>G rs768828257
NM_005982.4(SIX1):c.*755T>G rs868568764
NM_005982.4(SIX1):c.*765_*766del rs33943216
NM_005982.4(SIX1):c.-14G>T rs374228886
NM_005982.4(SIX1):c.-161G>C rs886050573
NM_005982.4(SIX1):c.-184A>C rs187402923
NM_005982.4(SIX1):c.-185T>C rs745791461
NM_005982.4(SIX1):c.-213C>G rs771815597
NM_005982.4(SIX1):c.-84C>G rs886050572
NM_005982.4(SIX1):c.822C>T (p.Pro274=) rs368353344

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