List of variants in gene MAP2K1 reported as benign for not specified

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_002755.4(MAP2K1):c.291+22G>C	rs16949924	0.27222
NM_002755.4(MAP2K1):c.1023-8C>T	rs41306345	0.09409
NM_002755.4(MAP2K1):c.438+20C>T	rs16949939	0.01567
NM_002755.4(MAP2K1):c.711G>A (p.Gly237=)	rs17586159	0.01226
NM_002755.4(MAP2K1):c.-2A>G	rs77796976	0.00820
NM_002755.4(MAP2K1):c.927A>T (p.Ala309=)	rs146869577	0.00357
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.6C>T (p.Pro2=)	rs377720622	0.00025
NM_002755.4(MAP2K1):c.237C>T (p.Gly79=)	rs148656020	0.00024
NM_002755.4(MAP2K1):c.636C>T (p.Ser212=)	rs138466751	0.00011
NM_002755.4(MAP2K1):c.439-19C>A	rs766207567	0.00010
NM_002755.4(MAP2K1):c.292-3C>T	rs55694358	0.00007
NM_002755.4(MAP2K1):c.569-19T>A	rs371099866	0.00006
NM_002755.4(MAP2K1):c.177G>A (p.Lys59=)	rs773928828	0.00003
NM_002755.4(MAP2K1):c.804C>G (p.Ala268=)	rs371652992	0.00001
NM_002755.4(MAP2K1):c.291+18A>T	rs577549188
NM_002755.4(MAP2K1):c.694-12TC[4]	rs113913469

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