List of variants in gene RIPK4 reported as benign by PreventionGenetics, part of Exact Sciences

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_020639.3(RIPK4):c.1996A>G (p.Met666Val)	rs3746891	0.98229
NM_020639.3(RIPK4):c.1548C>T (p.Asp516=)	rs2838113	0.53199
NM_020639.3(RIPK4):c.2331G>A (p.Thr777=)	rs7276592	0.41978
NM_020639.3(RIPK4):c.1476G>A (p.Ala492=)	rs3746893	0.41949
NM_020639.3(RIPK4):c.1203C>T (p.Gly401=)	rs3746894	0.41922
NM_020639.3(RIPK4):c.1005G>T (p.Leu335=)	rs2277789	0.38050
NM_020639.3(RIPK4):c.1884C>T (p.Ser628=)	rs55812846	0.00492
NM_020639.3(RIPK4):c.1617G>A (p.Thr539=)	rs61740535	0.00411
NM_020639.3(RIPK4):c.2214G>A (p.Ala738=)	rs150704061	0.00300
NM_020639.3(RIPK4):c.2070C>T (p.Val690=)	rs149475741	0.00232
NM_020639.3(RIPK4):c.2145C>T (p.His715=)	rs61739694	0.00090
NM_020639.3(RIPK4):c.2250G>A (p.Thr750=)	rs201024640	0.00023

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