List of variants in gene ROR2 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 44

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HGVS	dbSNP	gnomAD frequency
NM_004560.4(ROR2):c.*135G>T	rs774621355	0.00026
NM_004560.4(ROR2):c.-102G>T	rs932588990	0.00022
NM_004560.4(ROR2):c.871A>G (p.Met291Val)	rs150364724	0.00019
NM_004560.4(ROR2):c.1601C>A (p.Pro534His)	rs762554351	0.00013
NM_004560.4(ROR2):c.1885G>A (p.Val629Met)	rs148844963	0.00011
NM_004560.4(ROR2):c.1940A>G (p.Lys647Arg)	rs369059394	0.00011
NM_004560.4(ROR2):c.1624G>A (p.Val542Met)	rs140213020	0.00010
NM_004560.4(ROR2):c.1746G>A (p.Thr582=)	rs201241207	0.00010
NM_004560.4(ROR2):c.2782G>C (p.Asp928His)	rs199855010	0.00009
NM_004560.4(ROR2):c.1490C>T (p.Pro497Leu)	rs772631240	0.00008
NM_004560.4(ROR2):c.1240A>G (p.Ile414Val)	rs145023692	0.00007
NM_004560.4(ROR2):c.1105G>A (p.Gly369Arg)	rs151187583	0.00006
NM_004560.4(ROR2):c.1997A>G (p.Tyr666Cys)	rs1463489541	0.00006
NM_004560.4(ROR2):c.37C>G (p.Leu13Val)	rs1053014086	0.00006
NM_004560.4(ROR2):c.2521C>G (p.Gln841Glu)	rs771461100	0.00005
NM_004560.4(ROR2):c.1553G>A (p.Arg518Gln)	rs373544528	0.00004
NM_004560.4(ROR2):c.1630A>G (p.Thr544Ala)	rs374811924	0.00004
NM_004560.4(ROR2):c.1732G>A (p.Asp578Asn)	rs139802697	0.00004
NM_004560.4(ROR2):c.175+3G>T	rs557936422	0.00004
NM_004560.4(ROR2):c.1913G>A (p.Arg638Gln)	rs765278167	0.00004
NM_004560.4(ROR2):c.281G>A (p.Arg94Gln)	rs367829411	0.00004
NM_004560.4(ROR2):c.1552C>T (p.Arg518Trp)	rs148896640	0.00003
NM_004560.4(ROR2):c.1799C>T (p.Ala600Val)	rs143738026	0.00003
NM_004560.4(ROR2):c.1873G>A (p.Asp625Asn)	rs754476697	0.00003
NM_004560.4(ROR2):c.2080T>C (p.Cys694Arg)	rs142386992	0.00003
NM_004560.4(ROR2):c.1154G>A (p.Arg385His)	rs755135206	0.00002
NM_004560.4(ROR2):c.1399G>C (p.Glu467Gln)	rs780576494	0.00002
NM_004560.4(ROR2):c.1771G>A (p.Asp591Asn)	rs768175141	0.00002
NM_004560.4(ROR2):c.2206C>T (p.Arg736Trp)	rs1329621652	0.00002
NM_004560.4(ROR2):c.2354G>A (p.Arg785His)	rs368059807	0.00002
NM_004560.4(ROR2):c.1322G>A (p.Arg441Gln)	rs142993413	0.00001
NM_004560.4(ROR2):c.1502C>A (p.Thr501Asn)	rs142047260	0.00001
NM_004560.4(ROR2):c.1639C>A (p.Gln547Lys)	rs1489863862	0.00001
NM_004560.4(ROR2):c.1687G>A (p.Glu563Lys)	rs186571882	0.00001
NM_004560.4(ROR2):c.2155G>A (p.Ala719Thr)	rs375448033	0.00001
NM_004560.4(ROR2):c.302C>T (p.Pro101Leu)	rs370882834	0.00001
NM_004560.4(ROR2):c.334C>T (p.Arg112Trp)	rs868585233	0.00001
NM_004560.4(ROR2):c.457C>T (p.Arg153Trp)	rs745695427	0.00001
NM_004560.4(ROR2):c.533G>A (p.Arg178Gln)	rs746562213	0.00001
NM_004560.4(ROR2):c.768C>T (p.Cys256=)	rs772113008	0.00001
NM_004560.4(ROR2):c.769G>A (p.Glu257Lys)	rs543118807	0.00001
NM_004560.4(ROR2):c.904C>T (p.Arg302Cys)	rs767372181	0.00001
NM_004560.4(ROR2):c.1412C>T (p.Ser471Phe)	rs1564230209
NM_004560.4(ROR2):c.2014G>A (p.Asp672Asn)	rs55651110

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