ClinVar Miner

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

Included ClinVar conditions (325):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_005982.4(SIX1):c.*767A>T rs574976629 0.01905
NM_005982.4(SIX1):c.-137C>T rs139621918 0.00654
NM_005982.4(SIX1):c.-184A>C rs187402923 0.00127
NM_005982.4(SIX1):c.330G>A (p.Arg110=) rs73309461 0.00078
NM_005982.4(SIX1):c.*443A>G rs186530769 0.00053
NM_005982.4(SIX1):c.615T>G (p.Pro205=) rs148433316 0.00037
NM_005982.4(SIX1):c.578A>T (p.Asn193Ile) rs142301715 0.00032
NM_005982.4(SIX1):c.-14G>T rs374228886 0.00031
NM_005982.4(SIX1):c.162G>A (p.Ala54=) rs150550985 0.00031
NM_005982.4(SIX1):c.*1079T>A rs559116477 0.00024
NM_005982.4(SIX1):c.*1044G>T rs3742637 0.00014
NM_005982.4(SIX1):c.180C>G (p.Arg60=) rs781519092 0.00011
NM_005982.4(SIX1):c.474C>T (p.Ala158=) rs199743522 0.00008
NM_005982.4(SIX1):c.-24C>T rs201700039 0.00005
NM_005982.4(SIX1):c.690G>C (p.Ser230=) rs571997198 0.00005
NM_005982.4(SIX1):c.705G>T (p.Gln235His) rs747474509 0.00004
NM_005982.4(SIX1):c.720C>T (p.His240=) rs759290962 0.00004
NM_005982.4(SIX1):c.816C>T (p.Leu272=) rs750377629 0.00004
NM_005982.4(SIX1):c.465G>A (p.Arg155=) rs748903952 0.00002
NM_005982.4(SIX1):c.414C>T (p.Val138=) rs572940248 0.00001
NM_005982.4(SIX1):c.560+7G>C rs767884287 0.00001
NM_005982.4(SIX1):c.561-13C>T rs1894946571 0.00001
NM_005982.4(SIX1):c.854A>G (p.Ter285=) rs1894938537 0.00001
NM_005982.4(SIX1):c.138C>T (p.Asn46=)
NM_005982.4(SIX1):c.225C>T (p.Phe75=)
NM_005982.4(SIX1):c.228G>T (p.Ser76=)
NM_005982.4(SIX1):c.24C>G (p.Gly8=) rs770093951
NM_005982.4(SIX1):c.267G>A (p.Lys89=)
NM_005982.4(SIX1):c.357C>T (p.Arg119=) rs375984653
NM_005982.4(SIX1):c.447A>G (p.Pro149=)
NM_005982.4(SIX1):c.543C>G (p.Ala181=)
NM_005982.4(SIX1):c.561-19G>A
NM_005982.4(SIX1):c.570C>G (p.Thr190=)
NM_005982.4(SIX1):c.609C>T (p.Leu203=)
NM_005982.4(SIX1):c.696T>G (p.Leu232=)
NM_005982.4(SIX1):c.746C>A (p.Pro249Gln) rs368974927
NM_005982.4(SIX1):c.746C>T (p.Pro249Leu) rs368974927
NM_005982.4(SIX1):c.811C>T (p.Leu271=)
NM_005982.4(SIX1):c.849G>A (p.Gly283=)
NM_005982.4(SIX1):c.852C>T (p.Ser284=)

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