ClinVar Miner

List of variants studied for Primary hyperoxaluria by Sydney Genome Diagnostics,Children's Hospital Westmead

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Total variants: 3
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HGVS dbSNP
NM_000030.3(AGXT):c.1049G>A (p.Gly350Asp) rs180177156
NM_000030.3(AGXT):c.364C>T (p.Arg122Ter) rs180177210
NM_012203.2(GRHPR):c.295C>T (p.Arg99Ter) rs119490108

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