ClinVar Miner

List of variants in gene SLC30A7 reported as uncertain significance for not specified

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_133496.5(SLC30A7):c.566A>G (p.His189Arg) rs111335585 0.00042
NM_133496.5(SLC30A7):c.785G>A (p.Gly262Asp) rs140753374 0.00037
NM_133496.5(SLC30A7):c.1066C>A (p.His356Asn) rs538786032 0.00016
NM_133496.5(SLC30A7):c.461T>C (p.Ile154Thr) rs376713179 0.00004
NM_133496.5(SLC30A7):c.923G>A (p.Cys308Tyr) rs142163084 0.00003
NM_133496.5(SLC30A7):c.1084G>A (p.Ala362Thr) rs775789583 0.00001
NM_133496.5(SLC30A7):c.409C>T (p.His137Tyr) rs1652143982 0.00001
NM_133496.5(SLC30A7):c.662C>T (p.Pro221Leu) rs778818510 0.00001
NM_133496.5(SLC30A7):c.1121C>A (p.Ala374Glu)
NM_133496.5(SLC30A7):c.167G>C (p.Gly56Ala)
NM_133496.5(SLC30A7):c.172T>A (p.Trp58Arg) rs769981713
NM_133496.5(SLC30A7):c.278A>G (p.Asn93Ser)
NM_133496.5(SLC30A7):c.356C>A (p.Ala119Asp) rs2524634407
NM_133496.5(SLC30A7):c.515A>G (p.His172Arg) rs372301787
NM_133496.5(SLC30A7):c.547C>G (p.Leu183Val) rs2524648972
NM_133496.5(SLC30A7):c.565C>G (p.His189Asp) rs1252352176
NM_133496.5(SLC30A7):c.628C>T (p.His210Tyr)
NM_133496.5(SLC30A7):c.647A>G (p.His216Arg) rs1047924461
NM_133496.5(SLC30A7):c.696G>C (p.Gln232His) rs774836380
NM_133496.5(SLC30A7):c.791T>A (p.Met264Lys)
NM_133496.5(SLC30A7):c.847A>T (p.Ile283Phe)
NM_133496.5(SLC30A7):c.929A>G (p.Gln310Arg) rs1245755894

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