ClinVar Miner

List of variants in gene SIX1 studied for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP
NM_005982.4(SIX1):c.*1001T>C rs886050568
NM_005982.4(SIX1):c.*1008del rs148821608
NM_005982.4(SIX1):c.*1044G>T rs3742637
NM_005982.4(SIX1):c.*1079T>A rs559116477
NM_005982.4(SIX1):c.*1268_*1269AT[1] rs3832952
NM_005982.4(SIX1):c.*1496C>T rs61993831
NM_005982.4(SIX1):c.*1571T>C rs886050567
NM_005982.4(SIX1):c.*161C>A rs886050571
NM_005982.4(SIX1):c.*265del rs112733948
NM_005982.4(SIX1):c.*268_*271CAAA[2] rs886050570
NM_005982.4(SIX1):c.*297T>G rs147081368
NM_005982.4(SIX1):c.*334C>G rs10144415
NM_005982.4(SIX1):c.*371A>G rs538935374
NM_005982.4(SIX1):c.*404A>G rs76116881
NM_005982.4(SIX1):c.*443A>G rs186530769
NM_005982.4(SIX1):c.*578_*581del rs556041829
NM_005982.4(SIX1):c.*602G>C rs78909843
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.*766del rs33943216
NM_005982.4(SIX1):c.*767A>T rs574976629
NM_005982.4(SIX1):c.*883_*889CTAGTTT[1] rs561797428
NM_005982.4(SIX1):c.-121C>G rs375002099
NM_005982.4(SIX1):c.-137C>T rs139621918
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.-255G>T rs79926530
NM_005982.4(SIX1):c.-84C>G rs886050572
NM_005982.4(SIX1):c.162G>A (p.Ala54=) rs150550985
NM_005982.4(SIX1):c.180C>G (p.Arg60=) rs781519092
NM_005982.4(SIX1):c.317T>G (p.Val106Gly) rs397515560
NM_005982.4(SIX1):c.334C>T (p.Arg112Cys) rs397515561
NM_005982.4(SIX1):c.386A>G (p.Tyr129Cys) rs104894478
NM_005982.4(SIX1):c.50T>A (p.Val17Glu) rs397515562
NM_005982.4(SIX1):c.578A>T (p.Asn193Ile) rs142301715
NM_005982.4(SIX1):c.822C>T (p.Pro274=) rs368353344

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