ClinVar Miner

List of variants in gene SIX1 reported as benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_005982.4(SIX1):c.*1044G>T rs3742637
NM_005982.4(SIX1):c.*1079T>A rs559116477
NM_005982.4(SIX1):c.*1496C>T rs61993831
NM_005982.4(SIX1):c.*265del rs112733948
NM_005982.4(SIX1):c.*297T>G rs147081368
NM_005982.4(SIX1):c.*334C>G rs10144415
NM_005982.4(SIX1):c.*404A>G rs76116881
NM_005982.4(SIX1):c.*443A>G rs186530769
NM_005982.4(SIX1):c.*602G>C rs78909843
NM_005982.4(SIX1):c.*766del rs33943216
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.-184A>C rs187402923
NM_005982.4(SIX1):c.-24C>T
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.330G>A (p.Arg110=) rs73309461
NM_005982.4(SIX1):c.578A>T (p.Asn193Ile) rs142301715
NM_005982.4(SIX1):c.679G>T (p.Asp227Tyr) rs144481204

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