ClinVar Miner

List of variants in gene F8 reported as likely benign by Illumina Laboratory Services, Illumina

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Gene type:
ClinVar version:
Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_000132.4(F8):c.1508G>A (p.Arg503His) rs35383156 0.00563
NM_000132.4(F8):c.2994T>G (p.His998Gln) rs149853218 0.00419
NM_000132.4(F8):c.389-9C>T rs35621875 0.00356
NM_000132.4(F8):c.*1379A>G rs36101366 0.00127
NM_000132.4(F8):c.102C>T (p.Asp34=) rs1800283 0.00070
NM_000132.4(F8):c.*30G>A rs376482768 0.00020
NM_000132.4(F8):c.1064G>A (p.Arg355Gln) rs146581224 0.00019
NM_000132.4(F8):c.2383A>G (p.Arg795Gly) rs2228152 0.00016
NM_000132.4(F8):c.2212T>G (p.Tyr738Asp) rs201721215 0.00015
NM_000132.4(F8):c.3885C>G (p.Asn1295Lys) rs201393905 0.00009
NM_000132.4(F8):c.2217G>A (p.Glu739=) rs781850654 0.00005
NM_000132.4(F8):c.748A>G (p.Met250Val) rs781943293 0.00005
NM_000132.4(F8):c.2535C>A (p.Asp845Glu) rs200316756 0.00003
NM_000132.4(F8):c.3981G>A (p.Thr1327=) rs374245599 0.00002
NM_000132.4(F8):c.6957G>A (p.Pro2319=) rs200902529 0.00001
NM_000132.4(F8):c.*992A>G rs782499043
NM_000132.4(F8):c.4679C>G (p.Pro1560Arg) rs782791962

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