List of variants in gene KRAS reported as likely 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: 34

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HGVS	dbSNP	gnomAD frequency
NM_033360.4(KRAS):c.*1759A>G	rs4597149	0.99474
NM_033360.4(KRAS):c.*3907A>G	rs8720	0.48208
NM_033360.4(KRAS):c.*633T>C	rs9266	0.48177
NM_033360.4(KRAS):c.*3498C>T	rs1137188	0.48161
NM_033360.4(KRAS):c.*4022A>C	rs12587	0.48152
NM_033360.4(KRAS):c.*4200T>A	rs12245	0.48134
NM_033360.4(KRAS):c.*3522T>A	rs1137189	0.48000
NM_033360.4(KRAS):c.*3009A>G	rs13096	0.45974
NM_033360.4(KRAS):c.*298T>G	rs712	0.45514
NM_033360.4(KRAS):c.*3881A>C	rs1137196	0.36455
NM_004985.5(KRAS):c.519T>C (p.Asp173=)	rs1137282	0.19563
NM_033360.4(KRAS):c.*1708T>C	rs7973450	0.19546
NM_033360.4(KRAS):c.*1204A>G	rs7960917	0.18298
NM_033360.4(KRAS):c.*1776C>T	rs7973623	0.18240
NM_033360.4(KRAS):c.*2626T>G	rs61764370	0.06273
NM_033360.4(KRAS):c.*1094G>T	rs61763590	0.06270
NM_033360.4(KRAS):c.*2305A>G	rs61764368	0.04337
NM_033360.4(KRAS):c.*4432A>G	rs61764374	0.03798
NM_033360.4(KRAS):c.*3623T>A	rs61764372	0.02189
NM_033360.4(KRAS):c.*1886T>C	rs115968671	0.01694
NM_033360.4(KRAS):c.*3273G>A	rs61764371	0.01646
NM_033360.4(KRAS):c.*945T>C	rs61763589	0.01587
NM_033360.4(KRAS):c.*1183G>A	rs61763591	0.00998
NM_033360.4(KRAS):c.*525T>C	rs140080026	0.00652
NM_033360.4(KRAS):c.1758_1759del	rs535478558	0.00456
NM_033360.4(KRAS):c.*1661T>C	rs61764366	0.00455
NM_033360.4(KRAS):c.*2492C>T	rs61764369	0.00439
NM_033360.4(KRAS):c.1539_1541del	rs200038818
NM_033360.4(KRAS):c.*1748dup	rs71065923
NM_033360.4(KRAS):c.*2400dup	rs56128001
NM_033360.4(KRAS):c.*3385del	rs34176876
NM_033360.4(KRAS):c.*3804dup	rs142323886
NM_033360.4(KRAS):c.4186_4187del	rs34719539
NM_033360.4(KRAS):c.4426_4427dup	rs61764373

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