ClinVar Miner

List of variants reported as uncertain significance for Focal segmental glomerulosclerosis 9

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Total variants: 13
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HGVS dbSNP gnomAD frequency
NM_173689.7(CRB2):c.38C>T (p.Ala13Val) rs199695001 0.00046
NM_173689.7(CRB2):c.3746G>A (p.Arg1249Gln) rs147412276 0.00045
NM_173689.7(CRB2):c.1600C>T (p.Arg534Trp) rs759002273 0.00006
NM_173689.7(CRB2):c.3754C>T (p.Arg1252Cys) rs537738396 0.00006
NM_173689.7(CRB2):c.2741C>T (p.Ala914Val) rs1221877694 0.00003
NM_173689.7(CRB2):c.3190C>T (p.Pro1064Ser) rs868484209 0.00003
NM_173689.7(CRB2):c.3613G>A (p.Gly1205Ser) rs779586424 0.00003
NM_173689.7(CRB2):c.2914C>T (p.Arg972Cys) rs1236510733 0.00001
NM_173689.7(CRB2):c.3559A>C (p.Thr1187Pro) rs1554785663 0.00001
NM_173689.7(CRB2):c.1151G>T (p.Cys384Phe) rs1198089043
NM_173689.7(CRB2):c.2314C>G (p.Leu772Val) rs376152518
NM_173689.7(CRB2):c.2803G>C (p.Gly935Arg)
NM_173689.7(CRB2):c.429C>T (p.Cys143=) rs2041924139

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