Variants in gene CLN6 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 16

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HGVS	dbSNP	gnomAD frequency
NM_017882.3(CLN6):c.34G>A (p.Ala12Thr)	rs112239768	0.01081
NM_017882.3(CLN6):c.923G>C (p.Ser308Thr)	rs143578698	0.00169
NM_017882.3(CLN6):c.53C>T (p.Ala18Val)	rs547125345	0.00120
NM_017882.3(CLN6):c.487-15C>T	rs200775021	0.00049
NM_017882.3(CLN6):c.822G>A (p.Ala274=)	rs151186473	0.00041
NM_017882.3(CLN6):c.282C>A (p.Pro94=)	rs139261571	0.00021
NM_017882.3(CLN6):c.585C>T (p.Gly195=)	rs144507672	0.00011
NM_017882.3(CLN6):c.298-15C>T	rs368661456	0.00009
NM_017882.3(CLN6):c.199-5C>T	rs371705916	0.00006
NM_017882.3(CLN6):c.597C>G (p.Ala199=)	rs368546281	0.00006
NM_017882.3(CLN6):c.831C>T (p.Val277=)	rs753344266	0.00003
NM_017882.3(CLN6):c.49G>A (p.Gly17Ser)	rs763944821	0.00002
NM_017882.3(CLN6):c.*141GT[12]	rs3837692
NM_017882.3(CLN6):c.213C>G (p.Leu71=)	rs146980624
NM_017882.3(CLN6):c.66C>T (p.Ala22=)	rs796052349
NM_017882.3(CLN6):c.83+11G>A	rs2093262385

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