List of variants in gene NR2E3 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_014249.4(NR2E3):c.349+8G>A	rs112520386	0.00344
NM_014249.4(NR2E3):c.230G>A (p.Arg77Gln)	rs186714117	0.00087
NM_014249.4(NR2E3):c.170A>G (p.Lys57Arg)	rs563014885	0.00011
NM_014249.4(NR2E3):c.119-8C>T	rs373874970	0.00006
NM_014249.4(NR2E3):c.899C>T (p.Thr300Met)	rs374016332	0.00003
NM_014249.4(NR2E3):c.1127C>A (p.Pro376Gln)	rs527428190
NM_014249.4(NR2E3):c.1182C>T (p.Thr394=)	rs2140294988
NM_014249.4(NR2E3):c.568G>A (p.Asp190Asn)

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