List of variants in gene RORB 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_006914.4(RORB):c.418A>G (p.Thr140Ala)	rs151121778	0.00006
NM_006914.4(RORB):c.1225-4G>A	rs774246940	0.00002
NM_006914.4(RORB):c.488C>G (p.Pro163Arg)	rs766539793	0.00002
NM_006914.4(RORB):c.889T>G (p.Ser297Ala)	rs775164484	0.00001
NM_006914.4(RORB):c.1224G>A (p.Lys408=)
NM_006914.4(RORB):c.197G>C (p.Arg66Pro)
NM_006914.4(RORB):c.471C>G (p.Asn157Lys)
NM_006914.4(RORB):c.53C>T (p.Ser18Phe)
NM_006914.4(RORB):c.784T>C (p.Cys262Arg)	rs2118516548
NM_006914.4(RORB):c.835C>T (p.Arg279Trp)	rs1824205692
NM_006914.4(RORB):c.844G>A (p.Gly282Ser)
NM_006914.4(RORB):c.935A>G (p.Asn312Ser)	rs1824250701

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