ClinVar Miner

List of variants in gene USH1C reported as likely benign for Usher syndrome type 1C

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_005709.3(USH1C):c.1284+1133C>T rs377439949
NM_005709.3(USH1C):c.1284+7552A>G rs397517872
NM_005709.3(USH1C):c.1284+7580G>A rs780428813
NM_005709.3(USH1C):c.1285-7549C>T rs1554956913
NM_005709.3(USH1C):c.1285-7549delC rs1554956916
NM_005709.3(USH1C):c.1285-7567C>T rs727505247
NM_005709.3(USH1C):c.1518C>T (p.Asn506=) rs397517876
NM_005709.3(USH1C):c.1646+1080G>T rs571304936
NM_005709.3(USH1C):c.1646+1124C>T rs767767573
NM_005709.3(USH1C):c.1646+1151G>A rs201533059
NM_005709.3(USH1C):c.1647-1181G>A rs727504552
NM_005709.3(USH1C):c.582C>T (p.Gly194=) rs397517882
NM_153676.3(USH1C):c.2124T>C (p.Ser708=) rs369021714

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