List of variants in gene combination CBR4, PALLD reported as benign for digestive system disorder

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_001166108.2(PALLD):c.*2058C>G	rs1071738	0.51499
NM_001166108.2(PALLD):c.*1906G>A	rs1136603	0.13125
NM_001166108.2(PALLD):c.2679A>G (p.Arg893=)	rs1059444	0.12743
NM_001166108.2(PALLD):c.3359-4G>A	rs112116419	0.01852
NM_001166108.2(PALLD):c.*992A>G	rs28718025	0.01242
NM_001166108.2(PALLD):c.*1164T>G	rs114351964	0.01238
NM_001166108.2(PALLD):c.3297T>C (p.Tyr1099=)	rs114593924	0.00564
NM_001166108.2(PALLD):c.*492A>G	rs113794451	0.00224
NM_001166108.2(PALLD):c.2442A>G (p.Thr814=)	rs113676921	0.00218
NM_001166108.2(PALLD):c.33-4G>A	rs113515140	0.00105
NM_001166108.2(PALLD):c.*1594T>C	rs148023504	0.00102
NM_001166108.2(PALLD):c.2393T>C (p.Met798Thr)	rs142116575	0.00102
NM_001166108.2(PALLD):c.3256C>T (p.Leu1086=)	rs59633770	0.00098
NM_001166108.2(PALLD):c.*946C>A	rs76997292	0.00096
NM_001166108.2(PALLD):c.2199+8G>A	rs200060953	0.00070
NM_001166108.2(PALLD):c.*1829T>C	rs184106989	0.00046
NM_001166108.2(PALLD):c.2748C>T (p.Asp916=)	rs143544548	0.00039
NM_001166108.2(PALLD):c.2892T>C (p.Asp964=)	rs140584890	0.00028
NM_001166108.2(PALLD):c.2472+13A>G	rs190608408	0.00018
NM_001166108.2(PALLD):c.*994A>G	rs185646548	0.00014
NM_001166108.2(PALLD):c.2784T>C (p.Pro928=)	rs114250766	0.00010
NM_001166108.2(PALLD):c.*2214C>T	rs145960760	0.00001
NM_001166108.2(PALLD):c.*1132T>C	rs575893643
NM_001166108.2(PALLD):c.*2156del	rs398064261
NM_001166108.2(PALLD):c.*2162ATCA[2]	rs71719276
NM_001166108.2(PALLD):c.*325del	rs796761323
NM_001166108.2(PALLD):c.2199+5del	rs376654786
NM_001166108.2(PALLD):c.3150A>G (p.Val1050=)	rs781516286

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