Variants in gene KIF5A with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004984.4(KIF5A):c.967C>T (p.Arg323Trp)	rs1012819766	0.00001
NM_004984.4(KIF5A):c.2314C>T (p.Arg772Ter)	rs1555178616
NM_004984.4(KIF5A):c.484C>T (p.Arg162Trp)	rs748551786
NM_004984.4(KIF5A):c.610C>T (p.Arg204Trp)	rs1555177629
NM_004984.4(KIF5A):c.611G>A (p.Arg204Gln)	rs387907287
NM_004984.4(KIF5A):c.827A>G (p.Tyr276Cys)	rs121434443
NM_004984.4(KIF5A):c.838C>T (p.Arg280Cys)	rs121434442
NM_004984.4(KIF5A):c.839G>A (p.Arg280His)	rs387907288

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