List of variants in gene KCNJ8 reported as benign for cardiovascular disorder

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_004982.4(KCNJ8):c.291C>G (p.Ala97=)	rs34524779	0.01829
NM_004982.4(KCNJ8):c.1001T>C (p.Val334Ala)	rs34811413	0.01825
NM_004982.4(KCNJ8):c.855G>A (p.Leu285=)	rs34093632	0.01061
NM_004982.4(KCNJ8):c.793T>C (p.Leu265=)	rs16924297	0.00638
NM_004982.4(KCNJ8):c.897G>A (p.Val299=)	rs139329310	0.00088
NM_004982.4(KCNJ8):c.507C>T (p.Ile169=)	rs139304559	0.00051
NM_004982.4(KCNJ8):c.111C>T (p.Ile37=)	rs112604741	0.00021
NM_004982.4(KCNJ8):c.303C>T (p.Ile101=)	rs758633200	0.00004
NM_004982.4(KCNJ8):c.471G>A (p.Thr157=)	rs143319002
NM_004982.4(KCNJ8):c.66G>T (p.Leu22=)

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