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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 48

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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_000551.4(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.*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.*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.*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

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