ClinVar Miner

List of variants in gene ABCC6 reported as likely benign for not specified

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Gene type:
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Total variants: 17
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HGVS dbSNP
NM_001171.5(ABCC6):c.1077A>C (p.Ser359=) rs72664283
NM_001171.5(ABCC6):c.1141T>C (p.Leu381=) rs72664284
NM_001171.5(ABCC6):c.1248C>T (p.Asp416=) rs143487365
NM_001171.5(ABCC6):c.1263C>T (p.Thr421=) rs114179357
NM_001171.5(ABCC6):c.1815C>T (p.Leu605=) rs61318127
NM_001171.5(ABCC6):c.2820T>G (p.Arg940=) rs72664286
NM_001171.5(ABCC6):c.2836C>A (p.Leu946Ile) rs61340537
NM_001171.5(ABCC6):c.336C>A (p.Leu112=) rs971059840
NM_001171.5(ABCC6):c.3735+18G>A rs562368920
NM_001171.5(ABCC6):c.396A>G (p.Ser132=) rs913912489
NM_001171.5(ABCC6):c.4042-29G>A rs60810627
NM_001171.5(ABCC6):c.474+13G>A rs111339199
NM_001171.5(ABCC6):c.662+12C>T rs1555520951
NM_001171.5(ABCC6):c.754C>T (p.Leu252Phe) rs72653757
NM_001171.5(ABCC6):c.841A>G (p.Lys281Glu) rs879274205
NM_001171.5(ABCC6):c.855C>T (p.Thr285=) rs4780605
NM_001171.5(ABCC6):c.955A>G (p.Ile319Val) rs72657699

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