ClinVar Miner

List of variants reported as benign for Von Hippel-Lindau syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_000551.4(VHL):c.*1860A>G rs458106 0.98202
NM_000551.4(VHL):c.*2975G>C rs801913 0.90200
NM_000551.4(VHL):c.*3644_*3645insG rs201632485 0.86506
NM_000551.4(VHL):c.*1023G>A rs1681669 0.60118
NM_000551.4(VHL):c.*294G>A rs1642742 0.57360
NM_000551.4(VHL):c.*1060C>T rs1681668 0.57297
NM_000551.3(VHL):c.-195G>A rs779805 0.56161
NM_000551.4(VHL):c.*2548G>A rs187719061 0.12455
NM_000551.4(VHL):c.*2140C>T rs140614750 0.12149
NM_000551.4(VHL):c.*1973_*1979del rs149248243 0.12080
NM_000551.4(VHL):c.*2600T>A rs142728549 0.06248
NM_000551.4(VHL):c.*3523T>G rs17610448 0.02083
NM_000551.4(VHL):c.*724T>G rs13090104 0.01627
NM_000551.4(VHL):c.*3352G>A rs112130915 0.01140
NM_000551.4(VHL):c.*1990G>A rs113678809 0.01135
NM_000551.4(VHL):c.*1787G>A rs115303528 0.00645
NM_000551.4(VHL):c.*2201G>A rs145666034 0.00645
NM_000551.4(VHL):c.*1222A>G rs72563744 0.00642
NM_000551.4(VHL):c.*3453A>G rs140044688 0.00642
NM_000551.4(VHL):c.*1759A>G rs114732761 0.00641
NM_000551.4(VHL):c.*713T>C rs13090098 0.00641
NM_000551.4(VHL):c.*718T>C rs116182840 0.00641
NM_000551.4(VHL):c.*1328C>A rs78562649 0.00560
NM_000551.4(VHL):c.*1419A>G rs141916278 0.00551
NM_000551.4(VHL):c.*3603C>T rs145137834 0.00352
NM_000551.4(VHL):c.*3021T>C rs138933035 0.00296
NM_000551.4(VHL):c.74C>T (p.Pro25Leu) rs35460768 0.00261
NM_000551.4(VHL):c.*2594C>A rs191582744 0.00216
NM_000551.4(VHL):c.*3395C>T rs184144719 0.00205
NM_000551.4(VHL):c.*574T>C rs143062510 0.00195
NM_000551.4(VHL):c.340+5G>C rs61758376 0.00190
NM_000551.4(VHL):c.*820A>G rs182781943 0.00168
NM_000551.4(VHL):c.*1619T>C rs145608408 0.00154
NM_000551.4(VHL):c.*1947A>T rs546263769 0.00143
NM_000551.4(VHL):c.*2468C>T rs138237298 0.00109
NM_000551.4(VHL):c.150C>G (p.Ala50=) rs61751580 0.00070
NM_000551.4(VHL):c.*3617G>A rs527601820 0.00043
NM_000551.4(VHL):c.*1721C>G rs574191130 0.00037
NM_000551.4(VHL):c.*391C>T rs138178021 0.00022
NM_000551.4(VHL):c.*1680T>C rs561087293 0.00019
NM_000551.4(VHL):c.*2716G>A rs538719970 0.00018
NM_000551.4(VHL):c.*1867A>G rs566885734 0.00014
NM_000551.4(VHL):c.*70C>T rs552290225 0.00011
NM_000551.4(VHL):c.464-10G>A rs552930903 0.00006
NM_000551.4(VHL):c.*1452A>T rs552760935 0.00002
NM_000551.4(VHL):c.*303A>T rs573000980 0.00002
NM_000551.4(VHL):c.*2715C>T rs578053681 0.00001
NM_000551.4(VHL):c.*1181G>C rs72563745
NM_000551.4(VHL):c.*1301G>A rs541963428
NM_000551.4(VHL):c.*2034T>G rs1136249
NM_000551.4(VHL):c.*3097G>A rs149416955
NM_000551.4(VHL):c.*3482dup rs148013887
NM_000551.4(VHL):c.154G>A (p.Glu52Lys) rs373068386

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