List of variants in gene MAP2K1 reported as likely 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_002755.4(MAP2K1):c.315C>T (p.Pro105=)	rs144166521	0.00061
NM_002755.4(MAP2K1):c.69C>T (p.Thr23=)	rs140749690	0.00054
NM_002755.4(MAP2K1):c.237C>T (p.Gly79=)	rs148656020	0.00024
NM_002755.4(MAP2K1):c.726G>T (p.Val242=)	rs373745627	0.00013
NM_002755.4(MAP2K1):c.636C>T (p.Ser212=)	rs138466751	0.00011
NM_002755.4(MAP2K1):c.292-3C>T	rs55694358	0.00007
NM_002755.4(MAP2K1):c.957C>T (p.Asn319=)	rs143019052	0.00005
NM_002755.4(MAP2K1):c.439-8G>A	rs747709090	0.00004
NM_002755.4(MAP2K1):c.1023-20C>T	rs200542677	0.00003
NM_002755.4(MAP2K1):c.276G>C (p.Leu92=)	rs377323150	0.00003
NM_002755.4(MAP2K1):c.80+9G>A	rs1219385230	0.00003
NM_002755.4(MAP2K1):c.828G>A (p.Gly276=)

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