ClinVar Miner

List of variants in gene GCDH reported as likely benign for not provided

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_000159.4(GCDH):c.506-76C>T rs149381119 0.01444
NM_000159.4(GCDH):c.853-155G>A rs59033408 0.01296
NM_000159.4(GCDH):c.1243+303G>A rs116431183 0.00983
NM_000159.4(GCDH):c.334+247G>A rs114415076 0.00836
NM_000159.4(GCDH):c.1082+22C>T rs201346843 0.00281
NM_000159.4(GCDH):c.642G>A (p.Thr214=) rs142806397 0.00170
NM_000159.4(GCDH):c.271+3G>A rs75430014 0.00167
NM_000159.4(GCDH):c.1197C>T (p.His399=) rs139344943 0.00131
NM_000159.4(GCDH):c.1143C>T (p.Ile381=) rs142553521 0.00128
NM_000159.4(GCDH):c.471C>T (p.Ser157=) rs146682905 0.00081
NM_000159.4(GCDH):c.531C>T (p.Phe177=) rs144013229 0.00037
NM_000159.4(GCDH):c.627C>T (p.Thr209=) rs143172809 0.00016
NM_000159.4(GCDH):c.894G>A (p.Ala298=) rs150834108 0.00012
NM_000159.4(GCDH):c.886G>A (p.Gly296Ser) rs539505767 0.00009
NM_000159.4(GCDH):c.861C>T (p.Phe287=) rs200757991 0.00007
NM_000159.4(GCDH):c.396G>T (p.Arg132=) rs1160521098 0.00003
NM_000159.4(GCDH):c.1131A>G (p.Lys377=) rs139241235 0.00001
NM_000159.4(GCDH):c.506-194dup rs56251518
NM_000159.4(GCDH):c.771G>A (p.Arg257=) rs1599615127
NM_000159.4(GCDH):c.774C>T (p.Ala258=) rs1305712372

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