ClinVar Miner

List of variants reported as likely pathogenic for amyloidosis by 3billion

Included ClinVar conditions (40):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_021871.4(FGA):c.1690_1699dup (p.Ile567fs) rs1302701490 0.00001
NM_000371.4(TTR):c.425T>C (p.Val142Ala) rs2144414426
NM_198252.3(GSN):c.487G>T (p.Asp163Tyr) rs121909715

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