ClinVar Miner

List of variants in gene ZFYVE26 reported as likely pathogenic for Spastic paraplegia

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_015346.4(ZFYVE26):c.3139+1G>A rs137907310 0.00006
NM_015346.4(ZFYVE26):c.274-2A>G rs769329153 0.00002
NM_015346.4(ZFYVE26):c.3139+2T>G rs767164213 0.00002
NM_015346.4(ZFYVE26):c.1017+1G>T rs1224762841 0.00001
NM_015346.4(ZFYVE26):c.3020-2A>G rs1470672632 0.00001
NM_015346.4(ZFYVE26):c.5622-2A>G rs1272228031 0.00001
NC_000014.8:g.(?_68251766)_(68260966_?)del
NM_015346.4(ZFYVE26):c.1436-1G>A rs545219731
NM_015346.4(ZFYVE26):c.1639+1G>T
NM_015346.4(ZFYVE26):c.2332+1G>C
NM_015346.4(ZFYVE26):c.2401+2T>C
NM_015346.4(ZFYVE26):c.2553+1G>T
NM_015346.4(ZFYVE26):c.2554-1G>C rs760559263
NM_015346.4(ZFYVE26):c.2554-2A>G rs1186788102
NM_015346.4(ZFYVE26):c.2753_2755+5del
NM_015346.4(ZFYVE26):c.2756-1G>A rs2039758874
NM_015346.4(ZFYVE26):c.3139+1G>T rs137907310
NM_015346.4(ZFYVE26):c.3523+2T>C
NM_015346.4(ZFYVE26):c.3524-1G>C rs2140225441
NM_015346.4(ZFYVE26):c.3524-2A>G rs1555397331
NM_015346.4(ZFYVE26):c.4372+1_4372+3del rs1555396965
NM_015346.4(ZFYVE26):c.4674+2T>C
NM_015346.4(ZFYVE26):c.4675-2A>G
NM_015346.4(ZFYVE26):c.4797+2T>G rs2140215645
NM_015346.4(ZFYVE26):c.4798-1G>A rs1555396303
NM_015346.4(ZFYVE26):c.5222-1G>A rs2039307447
NM_015346.4(ZFYVE26):c.5485-1del rs878855013
NM_015346.4(ZFYVE26):c.5654-1G>A
NM_015346.4(ZFYVE26):c.5790+1G>A rs1340106074
NM_015346.4(ZFYVE26):c.5791-2A>G
NM_015346.4(ZFYVE26):c.6012-1G>A
NM_015346.4(ZFYVE26):c.6159+1G>A rs896655703
NM_015346.4(ZFYVE26):c.6160-2A>C
NM_015346.4(ZFYVE26):c.6369+1G>A rs1197046699
NM_015346.4(ZFYVE26):c.6786+1G>T
NM_015346.4(ZFYVE26):c.6987-1G>A rs1555393393
NM_015346.4(ZFYVE26):c.7188+1G>A rs1555393338
NM_015346.4(ZFYVE26):c.7188+1G>T rs1555393338
NM_015346.4(ZFYVE26):c.886+1G>T rs752618765
NM_015346.4(ZFYVE26):c.887-1G>C

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