List of variants in gene RIPK4 reported as benign by Illumina Laboratory Services, Illumina

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: 29

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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.*90T>C	rs6586232	0.79267
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.*560A>G	rs3746890	0.41259
NM_020639.3(RIPK4):c.782_783dup	rs34075882	0.40146
NM_020639.3(RIPK4):c.1005G>T (p.Leu335=)	rs2277789	0.38050
NM_020639.3(RIPK4):c.*983G>A	rs3171532	0.36576
NM_020639.3(RIPK4):c.35C>G (p.Ala12Gly)	rs6586239	0.15988
NM_020639.3(RIPK4):c.159G>A (p.Ser53=)	rs6586238	0.14219
NM_020639.3(RIPK4):c.360A>C (p.Arg120=)	rs13049286	0.13916
NM_020639.3(RIPK4):c.327T>C (p.Ala109=)	rs2277791	0.13904
NM_020639.3(RIPK4):c.1587G>A (p.Ser529=)	rs61740546	0.01687
NM_020639.3(RIPK4):c.1425G>A (p.Leu475=)	rs56092943	0.01339
NM_020639.3(RIPK4):c.117G>A (p.Val39=)	rs147023104	0.01319
NM_020639.3(RIPK4):c.7G>A (p.Gly3Ser)	rs199825512	0.01162
NM_020639.3(RIPK4):c.1311C>T (p.Ser437=)	rs56149248	0.01122
NM_020639.3(RIPK4):c.1119G>T (p.Gly373=)	rs61744790	0.01056
NM_020639.3(RIPK4):c.*707G>A	rs115461340	0.01049
NM_020639.3(RIPK4):c.*550C>G	rs113816274	0.00795
NM_020639.3(RIPK4):c.*1025G>T	rs73216989	0.00478
NM_020639.3(RIPK4):c.1617G>A (p.Thr539=)	rs61740535	0.00411
NM_020639.3(RIPK4):c.*747T>A	rs188837957	0.00375
NM_020639.3(RIPK4):c.303G>A (p.Thr101=)	rs2277792	0.00088
NM_020639.3(RIPK4):c.1980C>T (p.Gly660=)	rs144946647	0.00008
NM_020639.3(RIPK4):c.*215G>C	rs115041500
NM_020639.3(RIPK4):c.630G>C (p.Ala210=)	rs2838114

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