List of variants in gene KIF7 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: 26

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HGVS	dbSNP	gnomAD frequency
NM_198525.3(KIF7):c.1102A>G (p.Thr368Ala)	rs8037349	0.90740
NM_198525.3(KIF7):c.2658A>C (p.Ala886=)	rs3803531	0.85312
NM_198525.3(KIF7):c.1788+13T>C	rs1110060	0.59982
NM_198525.3(KIF7):c.3112-11_3112-10insCT	rs35820949	0.57089
NM_198525.3(KIF7):c.3048G>A (p.Ser1016=)	rs9672286	0.53592
NM_198525.3(KIF7):c.2896-14G>A	rs9672296	0.53577
NM_198525.3(KIF7):c.3013G>A (p.Gly1005Arg)	rs12900805	0.52523
NM_198525.3(KIF7):c.2873G>T (p.Ser958Ile)	rs3803530	0.52464
NM_198525.3(KIF7):c.*344T>C	rs1054435	0.41372
NM_198525.3(KIF7):c.154G>A (p.Asp52Asn)	rs8179065	0.20556
NM_198525.3(KIF7):c.1444-4A>G	rs112333674	0.02204
NM_198525.3(KIF7):c.216G>A (p.Gln72=)	rs113881220	0.02077
NM_198525.3(KIF7):c.*139C>T	rs8037511	0.01904
NM_198525.3(KIF7):c.2481C>T (p.Asn827=)	rs35837280	0.01186
NM_198525.3(KIF7):c.2271C>T (p.Ala757=)	rs35451920	0.00897
NM_198525.3(KIF7):c.1189G>A (p.Ala397Thr)	rs535621809	0.00887
NM_198525.3(KIF7):c.3012C>T (p.Arg1004=)	rs61741227	0.00828
NM_198525.3(KIF7):c.-52G>T	rs116805116	0.00808
NM_198525.3(KIF7):c.3999G>C (p.Pro1333=)	rs137993810	0.00730
NM_198525.3(KIF7):c.1266C>G (p.Leu422=)	rs8030837	0.00552
NM_198525.3(KIF7):c.1885G>A (p.Glu629Lys)	rs149814240	0.00533
NM_198525.3(KIF7):c.294A>G (p.Ser98=)	rs145049849	0.00465
NM_198525.3(KIF7):c.2981A>G (p.Gln994Arg)	rs138410949	0.00203
NM_198525.3(KIF7):c.1177G>T (p.Gly393Cys)	rs553968087	0.00007
NM_198525.3(KIF7):c.195G>C (p.Ala65=)	rs8179066
NM_198525.3(KIF7):c.2592+11C>A	rs78199895

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