Variants in gene MAP2K1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 16

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HGVS	dbSNP	gnomAD frequency
NM_002755.4(MAP2K1):c.711G>A (p.Gly237=)	rs17586159	0.01226
NM_002755.4(MAP2K1):c.648C>T (p.Ile216=)	rs148968935	0.00123
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.848C>T (p.Ala283Val)	rs144080051	0.00029
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.396G>A (p.Ala132=)	rs139364105	0.00006
NM_002755.4(MAP2K1):c.439-8G>A	rs747709090	0.00004
NM_002755.4(MAP2K1):c.156C>T (p.Ala52=)	rs147489724	0.00003
NM_002755.4(MAP2K1):c.276G>C (p.Leu92=)	rs377323150	0.00003
NM_002755.4(MAP2K1):c.900C>T (p.Tyr300=)	rs147333830	0.00002
NM_002755.4(MAP2K1):c.694-12TC[4]	rs113913469

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