List of variants in gene REEP6 reported as uncertain significance by Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_138393.4(REEP6):c.469G>A (p.Asp157Asn)	rs145541565	0.00096
NM_001329556.3(REEP6):c.535C>T (p.Arg179Cys)	rs529651864	0.00009
NM_001329556.3(REEP6):c.557C>T (p.Pro186Leu)	rs770429286
NM_138393.4(REEP6):c.157G>A (p.Gly53Arg)	rs756089270
NM_138393.4(REEP6):c.244G>A (p.Asp82Asn)	rs2084998620

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