ClinVar Miner

List of variants in gene CHST6 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_021615.5(CHST6):c.*1967C>T rs42967 0.97576
NM_021615.5(CHST6):c.*5286A>T rs9923834 0.82602
NM_021615.5(CHST6):c.*5445G>A rs10871313 0.66442
NM_021615.5(CHST6):c.*242_*243insG rs11436257 0.58387
NM_021615.5(CHST6):c.*3819G>C rs8063068 0.54358
NM_021615.5(CHST6):c.*1919C>T rs7194035 0.52511
NM_021615.5(CHST6):c.*2024C>G rs7193828 0.52124
NM_021615.5(CHST6):c.*4305T>C rs11641249 0.51737
NM_021615.5(CHST6):c.*1566T>G rs4888432 0.50768
NM_021615.5(CHST6):c.*3742C>T rs56116092 0.47041
NM_021615.5(CHST6):c.*4366T>C rs37606 0.38416
NM_021615.5(CHST6):c.*2327C>T rs185053 0.19705
NM_021615.5(CHST6):c.*4086G>A rs12918234 0.15036
NM_021615.5(CHST6):c.*955C>T rs116535181 0.03535
NM_021615.5(CHST6):c.*2288T>G rs147960476 0.02929
NM_021615.5(CHST6):c.*3992T>C rs8063344 0.02920
NM_021615.5(CHST6):c.*3828A>T rs56769615 0.02061
NM_021615.5(CHST6):c.*1426C>A rs11861434 0.01725
NM_021615.5(CHST6):c.*2956G>A rs11860278 0.01509
NM_021615.5(CHST6):c.258A>C (p.Ala86=) rs61740901 0.01353
NM_021615.5(CHST6):c.*5441C>T rs74742116 0.01333
NM_021615.5(CHST6):c.*377G>A rs138647317 0.01173
NM_021615.5(CHST6):c.120C>T (p.Arg40=) rs61740904 0.01016
NM_021615.5(CHST6):c.768C>T (p.Ala256=) rs146465655 0.00857
NM_021615.5(CHST6):c.*5187T>G rs28710075 0.00653
NM_021615.5(CHST6):c.*3621A>G rs139900788 0.00630
NM_021615.5(CHST6):c.*606G>A rs117741124 0.00621
NM_021615.5(CHST6):c.465G>A (p.Arg155=) rs141905571 0.00619
NM_021615.5(CHST6):c.294C>G (p.Ser98=) rs118144424 0.00618
NM_021615.5(CHST6):c.*2833T>G rs149981556 0.00595
NM_021615.5(CHST6):c.*991A>G rs142368532 0.00492
NM_021615.5(CHST6):c.*4155C>T rs114790233 0.00398
NM_021615.5(CHST6):c.129G>A (p.Val43=) rs112939575 0.00366
NM_021615.5(CHST6):c.*3465T>C rs76471046 0.00364
NM_021615.5(CHST6):c.666C>T (p.Asn222=) rs148529501 0.00284
NM_021615.5(CHST6):c.*3750C>A rs142693604 0.00220
NM_021615.5(CHST6):c.828G>A (p.Leu276=) rs140327212 0.00085
NM_021615.5(CHST6):c.*5465C>T rs541989548 0.00001
NM_021615.5(CHST6):c.*1047G>T rs77687996
NM_021615.5(CHST6):c.*1058G>A rs137868909
NM_021615.5(CHST6):c.*1375G>A rs116020927
NM_021615.5(CHST6):c.*1892del rs35225560
NM_021615.5(CHST6):c.*3223CT[1] rs5817947
NM_021615.5(CHST6):c.*4605C>T rs150105169
NM_021615.5(CHST6):c.484C>G (p.Arg162Gly) rs117435647

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