ClinVar Miner

Variants in gene SZT2 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 15
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HGVS dbSNP
NM_001365999.1(SZT2):c.1272A>G (p.Gln424=) rs780157180
NM_001365999.1(SZT2):c.2887A>G (p.Lys963Glu) rs753130543
NM_001365999.1(SZT2):c.2930-5C>T rs548527248
NM_001365999.1(SZT2):c.3638G>A (p.Arg1213His) rs187427261
NM_001365999.1(SZT2):c.4647C>T (p.Gly1549=) rs149192929
NM_001365999.1(SZT2):c.4727G>A (p.Arg1576His) rs143935839
NM_001365999.1(SZT2):c.4898C>T (p.Ser1633Leu) rs138762270
NM_001365999.1(SZT2):c.5377G>A (p.Glu1793Lys) rs143185010
NM_001365999.1(SZT2):c.5772G>T (p.Leu1924=) rs187188981
NM_001365999.1(SZT2):c.6343C>G (p.Pro2115Ala) rs147309177
NM_001365999.1(SZT2):c.6380A>T (p.Tyr2127Phe) rs149812437
NM_001365999.1(SZT2):c.6977G>A (p.Arg2326Gln) rs146140125
NM_001365999.1(SZT2):c.7474C>T (p.Arg2492Trp) rs373062274
NM_001365999.1(SZT2):c.8255G>A (p.Arg2752His) rs150591561
NM_001365999.1(SZT2):c.8916+8G>A rs147419780

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