ClinVar Miner

List of variants in gene ROR2 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_004560.4(ROR2):c.*16G>A rs2230578 0.73170
NM_004560.4(ROR2):c.2455G>A (p.Val819Ile) rs10761129 0.71630
NM_004560.4(ROR2):c.494+25G>A rs12683181 0.68697
NM_004560.4(ROR2):c.733A>G (p.Thr245Ala) rs10820900 0.66416
NM_004560.4(ROR2):c.2088C>T (p.Tyr696=) rs10992063 0.44353
NM_004560.4(ROR2):c.98-15G>C rs7863557 0.22863
NM_004560.4(ROR2):c.938-33C>T rs10992070 0.09787
NM_004560.4(ROR2):c.498T>C (p.Asp166=) rs16907720 0.09084
NM_004560.4(ROR2):c.2154C>T (p.Pro718=) rs2230577 0.05836
NM_004560.4(ROR2):c.1710G>A (p.Pro570=) rs41277837 0.02804
NM_004560.4(ROR2):c.937+10C>T rs201083970 0.00310
NM_004560.4(ROR2):c.372C>T (p.Asp124=) rs145568368 0.00241
NM_004560.4(ROR2):c.1686C>T (p.His562=) rs56048121 0.00232
NM_004560.4(ROR2):c.2395C>T (p.Pro799Ser) rs141235720 0.00173
NM_004560.4(ROR2):c.1184-39A>T rs147441352 0.00106
NM_004560.4(ROR2):c.1736A>T (p.Asp579Val) rs150610444 0.00092
NM_004560.4(ROR2):c.2461G>A (p.Val821Ile) rs149056068 0.00086
NM_004560.4(ROR2):c.1491G>A (p.Pro497=) rs146347005 0.00029
NM_004560.4(ROR2):c.751C>T (p.Leu251=) rs368471121 0.00025
NM_004560.4(ROR2):c.2694G>C (p.Gln898His) rs141070315 0.00017
NM_004560.4(ROR2):c.1524G>A (p.Thr508=) rs114395148 0.00013
NM_004560.4(ROR2):c.986G>A (p.Ser329Asn) rs371221714 0.00013
NM_004560.4(ROR2):c.1137G>A (p.Thr379=) rs767456619 0.00009
NM_004560.4(ROR2):c.744G>A (p.Pro248=) rs757948078 0.00009
NM_004560.4(ROR2):c.935G>A (p.Arg312His) rs188376581 0.00007
NM_004560.4(ROR2):c.1756G>A (p.Ala586Thr) rs142386294 0.00006
NM_004560.4(ROR2):c.1863G>A (p.Val621=) rs778321761 0.00006
NM_004560.4(ROR2):c.2212C>T (p.Arg738Cys) rs56231927 0.00006
NM_004560.4(ROR2):c.2445G>A (p.Pro815=) rs202010959 0.00006
NM_004560.4(ROR2):c.37C>G (p.Leu13Val) rs1053014086 0.00006
NM_004560.4(ROR2):c.153C>T (p.Asp51=) rs572950289 0.00004
NM_004560.4(ROR2):c.1770C>T (p.Pro590=) rs372398011 0.00004
NM_004560.4(ROR2):c.888C>T (p.Asp296=) rs755825636 0.00004
NM_004560.4(ROR2):c.435C>T (p.Thr145=) rs779139938 0.00001
NM_004560.4(ROR2):c.1323G>A (p.Arg441=) rs764898597
NM_004560.4(ROR2):c.1674C>T (p.His558=)
NM_004560.4(ROR2):c.2304G>A (p.Thr768=)
NM_004560.4(ROR2):c.2429C>T (p.Pro810Leu)
NM_004560.4(ROR2):c.2632C>G (p.Pro878Ala)
NM_004560.4(ROR2):c.2645C>G (p.Ser882Cys)
NM_004560.4(ROR2):c.2729A>G (p.Gln910Arg)
NM_004560.4(ROR2):c.725G>A (p.Arg242His) rs756285939
NM_004560.4(ROR2):c.762C>T (p.Asp254=)

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