ClinVar Miner

List of variants in gene LRP4 reported as uncertain significance for not provided

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Gene type:
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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_002334.4(LRP4):c.1048+7G>T rs148557097 0.00220
NM_002334.4(LRP4):c.639C>T (p.Asp213=) rs144974139 0.00124
NM_002334.4(LRP4):c.5660C>G (p.Ser1887Cys) rs149082597 0.00111
NM_002334.4(LRP4):c.3064A>G (p.Asn1022Asp) rs61742871 0.00098
NM_002334.4(LRP4):c.3620A>G (p.Asn1207Ser) rs151234321 0.00086
NM_002334.4(LRP4):c.257G>A (p.Arg86His) rs138239756 0.00083
NM_002334.4(LRP4):c.570C>T (p.Pro190=) rs147353838 0.00061
NM_002334.4(LRP4):c.1194A>G (p.Glu398=) rs138589242 0.00058
NM_002334.4(LRP4):c.5182A>G (p.Ile1728Val) rs148865136 0.00045
NM_002334.4(LRP4):c.3407G>A (p.Arg1136Gln) rs61736853 0.00042
NM_002334.4(LRP4):c.3944C>T (p.Ser1315Leu) rs150681693 0.00042
NM_002334.4(LRP4):c.4699A>T (p.Arg1567Trp) rs199747378 0.00041
NM_002334.4(LRP4):c.4936C>T (p.Arg1646Trp) rs141213903 0.00038
NM_002334.4(LRP4):c.1832G>A (p.Arg611His) rs140282454 0.00036
NM_002334.4(LRP4):c.2815-6T>G rs372210790 0.00030
NM_002334.4(LRP4):c.1130A>G (p.Gln377Arg) rs139006210 0.00024
NM_002334.4(LRP4):c.539A>G (p.Glu180Gly) rs201957426 0.00019
NM_002334.4(LRP4):c.1654A>T (p.Asn552Tyr) rs201253200 0.00018
NM_002334.4(LRP4):c.695G>A (p.Arg232His) rs370407081 0.00016
NM_002334.4(LRP4):c.1769G>A (p.Arg590His) rs149435615 0.00013
NM_002334.4(LRP4):c.3980G>A (p.Arg1327Gln) rs146372809 0.00010
NM_002334.4(LRP4):c.3073G>C (p.Gly1025Arg) rs141565454 0.00009
NM_002334.4(LRP4):c.4317C>T (p.Ala1439=) rs376909913 0.00009
NM_002334.4(LRP4):c.5489G>A (p.Arg1830Gln) rs146864522 0.00009
NM_002334.4(LRP4):c.70G>A (p.Glu24Lys) rs200465829 0.00009
NM_002334.4(LRP4):c.3940G>A (p.Gly1314Ser) rs371961330 0.00008
NM_002334.4(LRP4):c.4183G>A (p.Val1395Met) rs774275092 0.00008
NM_002334.4(LRP4):c.4075T>A (p.Ser1359Thr) rs775159238 0.00007
NM_002334.4(LRP4):c.5054G>A (p.Arg1685Gln) rs138238230 0.00007
NM_002334.4(LRP4):c.5513G>A (p.Arg1838Gln) rs770309253 0.00006
NM_002334.4(LRP4):c.909C>G (p.Asn303Lys) rs373551790 0.00006
NM_002334.4(LRP4):c.4898C>T (p.Ser1633Leu) rs146362081 0.00005
NM_002334.4(LRP4):c.5672C>T (p.Thr1891Met) rs372637156 0.00005
NM_002334.4(LRP4):c.1481G>A (p.Arg494His) rs777801967 0.00004
NM_002334.4(LRP4):c.761C>T (p.Ala254Val) rs767281769 0.00004
NM_002334.4(LRP4):c.1825G>A (p.Gly609Arg) rs1389594811 0.00003
NM_002334.4(LRP4):c.2515C>T (p.Arg839Trp) rs148910063 0.00003
NM_002334.4(LRP4):c.2767G>A (p.Gly923Ser) rs765716290 0.00002
NM_002334.4(LRP4):c.4082G>A (p.Arg1361His) rs779038341 0.00002
NM_002334.4(LRP4):c.5330A>C (p.Lys1777Thr) rs541585714 0.00002
NM_002334.4(LRP4):c.2010G>A (p.Thr670=) rs199654257 0.00001
NM_002334.4(LRP4):c.2243G>A (p.Arg748Gln) rs545112106 0.00001
NM_002334.4(LRP4):c.278A>G (p.Asp93Gly) rs1231831456 0.00001
NM_002334.4(LRP4):c.390T>C (p.Asp130=) rs140186161 0.00001
NM_002334.4(LRP4):c.4154A>G (p.Asn1385Ser) rs768733310 0.00001
NM_002334.4(LRP4):c.4361C>T (p.Ala1454Val) rs746692504 0.00001
NM_002334.4(LRP4):c.4503G>C (p.Leu1501Phe) rs375220795 0.00001
NM_002334.4(LRP4):c.5071G>A (p.Glu1691Lys) rs528376810 0.00001
NM_002334.4(LRP4):c.956G>A (p.Cys319Tyr) rs769749835 0.00001
NM_002334.4(LRP4):c.1031G>A (p.Ser344Asn)
NM_002334.4(LRP4):c.2119G>A (p.Gly707Arg) rs1382055371
NM_002334.4(LRP4):c.2348G>A (p.Arg783Gln)
NM_002334.4(LRP4):c.2428G>A (p.Val810Ile) rs1246395979
NM_002334.4(LRP4):c.248G>T (p.Cys83Phe) rs1565801283
NM_002334.4(LRP4):c.2725G>C (p.Ala909Pro)
NM_002334.4(LRP4):c.2815-11G>A rs2134808584
NM_002334.4(LRP4):c.3179G>T (p.Arg1060Leu) rs1941046156
NM_002334.4(LRP4):c.3266A>T (p.Asp1089Val)
NM_002334.4(LRP4):c.3278-141A>G rs1941036879
NM_002334.4(LRP4):c.3698A>C (p.Glu1233Ala) rs1940998166
NM_002334.4(LRP4):c.4148A>G (p.Glu1383Gly) rs202151304
NM_002334.4(LRP4):c.4322A>G (p.Asn1441Ser) rs886048350
NM_002334.4(LRP4):c.4511C>T (p.Ser1504Phe) rs1565780905
NM_002334.4(LRP4):c.4535C>G (p.Thr1512Arg)
NM_002334.4(LRP4):c.4937G>T (p.Arg1646Leu) rs3816614
NM_002334.4(LRP4):c.530C>A (p.Ser177Tyr) rs1565800416
NM_002334.4(LRP4):c.5438T>C (p.Ile1813Thr) rs991397044
NM_002334.4(LRP4):c.5456A>T (p.Asp1819Val) rs886043837
NM_002334.4(LRP4):c.5504dup (p.Leu1836fs)
NM_002334.4(LRP4):c.5662_5663del (p.Leu1888fs) rs770837962
NM_002334.4(LRP4):c.923-8CT[2]

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