ClinVar Miner

List of variants in gene combination GH-LCR, GH1 reported as uncertain significance by Eurofins NTD LLC (GA)

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Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_000515.5(GH1):c.15C>T (p.Ser5=) rs111957225 0.00107
NM_000515.5(GH1):c.597C>G (p.Val199=) rs142704768 0.00029
NM_000515.5(GH1):c.217A>G (p.Asn73Asp) rs71640276 0.00027
NM_000515.5(GH1):c.547C>T (p.Leu183Phe) rs184640372 0.00015
NM_000515.5(GH1):c.387C>T (p.Tyr129=) rs370785603 0.00009
NM_000515.5(GH1):c.370G>A (p.Ala124Thr) rs373958758 0.00003
NM_000515.5(GH1):c.16C>A (p.Arg6=) rs140576665
NM_000515.5(GH1):c.615C>G (p.Ile205Met) rs148474991

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