ClinVar Miner

List of variants in gene FGFR2 reported as uncertain significance by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Total variants: 9
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HGVS dbSNP
NM_022970.3(FGFR2):c.1089G>C (p.Ala363=) rs151250769
NM_022970.3(FGFR2):c.1208A>G (p.Asn403Ser) rs764748528
NM_022970.3(FGFR2):c.2043C>T (p.Tyr681=) rs751495618
NM_022970.3(FGFR2):c.2073G>T (p.Gly691=) rs1281525856
NM_022970.3(FGFR2):c.2109G>A (p.Ser703=) rs794727163
NM_022970.3(FGFR2):c.2127C>T (p.Pro709=) rs140813163
NM_022970.3(FGFR2):c.289G>A (p.Ala97Thr) rs372430349
NM_022970.3(FGFR2):c.568C>T (p.Arg190Trp) rs147987917
NM_022970.3(FGFR2):c.759T>G (p.Pro253=) rs3135755

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