ClinVar Miner

List of variants in gene combination LOC107303340, VHL reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_000551.3(VHL):c.*1465C>A rs183067022
NM_000551.3(VHL):c.*1960G>A rs9822696
NM_000551.3(VHL):c.*3492_*3493dup rs112494627
NM_000551.3(VHL):c.*523del rs546118793
NM_000551.3(VHL):c.*823G>A rs7629500
NM_000551.3(VHL):c.341-5G>A rs372340900
NM_000551.3(VHL):c.544A>G (p.Arg182Gly) rs778205243
NM_000551.3(VHL):c.599G>A (p.Arg200Gln) rs754016774
NM_000551.3(VHL):c.631A>C (p.Met211Leu) rs200019083
NM_198156.3(VHL):c.*923_*927GTTTT[5] rs544983652

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