ClinVar Miner

List of variants in gene APOB reported as likely benign by Color Diagnostics, LLC DBA Color Health

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.12794T>C (p.Val4265Ala) rs61743502 0.00516
NM_000384.3(APOB):c.3383G>A (p.Arg1128His) rs12713843 0.00356
NM_000384.3(APOB):c.7615G>A (p.Val2539Ile) rs148170480 0.00210
NM_000384.3(APOB):c.751G>A (p.Ala251Thr) rs61741625 0.00190
NM_000384.3(APOB):c.905-16A>C rs12720810 0.00172
NM_000384.3(APOB):c.7152T>C (p.Val2384=) rs72653090 0.00041
NM_000384.3(APOB):c.288G>T (p.Gln96His) rs186544754 0.00012
NM_000384.3(APOB):c.8877G>A (p.Leu2959=) rs765899256 0.00012
NM_000384.3(APOB):c.13095C>T (p.Asn4365=) rs13306203 0.00005
NM_000384.3(APOB):c.8720G>A (p.Arg2907His) rs751437976 0.00004
NM_000384.3(APOB):c.403A>G (p.Ile135Val) rs769296548 0.00001
NM_000384.3(APOB):c.10294C>G (p.Gln3432Glu)
NM_000384.3(APOB):c.10581G>C (p.Arg3527=)
NM_000384.3(APOB):c.11477C>T (p.Thr3826Met)
NM_000384.3(APOB):c.12940A>G (p.Ile4314Val)
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser)
NM_000384.3(APOB):c.5066G>A (p.Arg1689His)
NM_000384.3(APOB):c.7285T>A (p.Ser2429Thr)
NM_000384.3(APOB):c.9835A>G (p.Ser3279Gly)

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