ClinVar Miner

List of variants in gene combination LOC107303340, VHL reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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NM_000551.3(VHL):c.*1023G>A rs1681669
NM_000551.3(VHL):c.*1060C>T rs1681668
NM_000551.3(VHL):c.*1860A>G rs458106
NM_000551.3(VHL):c.*1973_*1979del rs149248243
NM_000551.3(VHL):c.*2034T>G rs1136249
NM_000551.3(VHL):c.*2140C>T rs140614750
NM_000551.3(VHL):c.*2548G>A rs187719061
NM_000551.3(VHL):c.*2600T>A rs142728549
NM_000551.3(VHL):c.*294G>A rs1642742
NM_000551.3(VHL):c.*2975G>C rs801913
NM_000551.3(VHL):c.*3482dup rs148013887
NM_000551.3(VHL):c.*3644_*3645insG rs201632485
NM_000551.3(VHL):c.538A>G (p.Ile180Val) rs377715747

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