List of variants in gene CHST6 reported as likely 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_021615.5(CHST6):c.-78T>C	rs114012239	0.01207
NM_021615.5(CHST6):c.*2955C>T	rs76087215	0.01047
NM_021615.5(CHST6):c.*3883T>G	rs138114811	0.00736
NM_021615.5(CHST6):c.*2426T>C	rs142614349	0.00365
NM_021615.5(CHST6):c.*1914A>G	rs143764747	0.00259
NM_021615.5(CHST6):c.*3917G>A	rs180746384	0.00250
NM_021615.5(CHST6):c.237C>T (p.Thr79=)	rs112148613	0.00247
NM_021615.5(CHST6):c.130C>T (p.Leu44=)	rs140675009	0.00219
NM_021615.5(CHST6):c.*2947G>T	rs112154704	0.00217
NM_021615.5(CHST6):c.*2210C>G	rs111315694	0.00216
NM_021615.5(CHST6):c.*4880G>A	rs76741848	0.00104
NM_021615.5(CHST6):c.*2417C>T	rs188632926	0.00080
NM_021615.5(CHST6):c.*5197C>T	rs554016597	0.00021
NM_021615.5(CHST6):c.*1118A>G	rs191429909	0.00014
NM_021615.5(CHST6):c.*435C>T	rs375230497	0.00013
NM_021615.5(CHST6):c.*1377G>A	rs140231054	0.00002
NM_021615.5(CHST6):c.*3364C>A	rs189970730
NM_021615.5(CHST6):c.*4487C>T	rs182168641

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