List of variants in gene combination KLLN, PTEN reported as uncertain significance by Quest Diagnostics Nichols Institute San Juan Capistrano

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001126049.2(KLLN):c.-644A>T	rs769351955	0.00005
NM_001126049.2(KLLN):c.-806A>C	rs587782761	0.00004
NM_001126049.2(KLLN):c.-846C>T	rs1042841710	0.00004
NM_001126049.2(KLLN):c.-775C>G	rs876661005	0.00003
NM_001126049.2(KLLN):c.-810C>T	rs587781548	0.00001
NM_001126049.2(KLLN):c.-870T>C	rs1173979974	0.00001
NM_001126049.2(KLLN):c.-677A>T	rs1554889777
NM_001126049.2(KLLN):c.-695dup	rs1589593475
NM_001126049.2(KLLN):c.-739C>T	rs727502790
NM_001126049.2(KLLN):c.-747G>C
NM_001126049.2(KLLN):c.-759del
NM_001126049.2(KLLN):c.-761C>G	rs965758202
NM_001126049.2(KLLN):c.-770C>A	rs998222631
NM_001126049.2(KLLN):c.-801C>A	rs1389966419
NM_001126049.2(KLLN):c.-812G>A	rs587779981
NM_001126049.2(KLLN):c.-862A>G	rs1554889848
NM_001126049.2(KLLN):c.-881G>A	rs1858324006

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