ClinVar Miner

List of variants in gene combination HSPG2, LDLRAD2 reported as uncertain significance for not provided

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Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_005529.7(HSPG2):c.13088C>T (p.Ser4363Leu) rs62642502 0.00312
NM_005529.7(HSPG2):c.12874G>A (p.Glu4292Lys) rs141280063 0.00135
NM_005529.7(HSPG2):c.13018G>A (p.Val4340Met) rs145687082 0.00106
NM_005529.7(HSPG2):c.13145C>A (p.Ala4382Asp) rs116316900 0.00079
NM_005529.7(HSPG2):c.13033G>A (p.Gly4345Arg) rs148788926 0.00045
NM_005529.7(HSPG2):c.12607G>A (p.Gly4203Arg) rs199814977 0.00041
NM_005529.7(HSPG2):c.13004-5G>A rs376645617 0.00031
NM_005529.7(HSPG2):c.12886G>C (p.Val4296Leu) rs144217842 0.00026
NM_005529.7(HSPG2):c.12929A>C (p.Asp4310Ala) rs144864169 0.00026
NM_005529.7(HSPG2):c.*103G>A rs777311066 0.00012
NM_005529.7(HSPG2):c.12884G>A (p.Arg4295Gln) rs537908254 0.00012
NM_005529.7(HSPG2):c.13153A>G (p.Asn4385Asp) rs752793818 0.00010
NM_005529.7(HSPG2):c.13098C>T (p.Pro4366=) rs759562639 0.00007
NM_005529.7(HSPG2):c.13172C>T (p.Ser4391Leu) rs961325868 0.00006
NM_005529.7(HSPG2):c.13006G>A (p.Gly4336Arg) rs550270875 0.00005
NM_005529.7(HSPG2):c.13147G>A (p.Gly4383Arg) rs554059442 0.00005
NM_005529.7(HSPG2):c.13096C>T (p.Pro4366Ser) rs771945509 0.00004
NM_005529.7(HSPG2):c.12691G>A (p.Glu4231Lys) rs374870276 0.00003
NM_005529.7(HSPG2):c.12907C>T (p.Arg4303Cys) rs761987723 0.00003
NM_005529.7(HSPG2):c.12949G>A (p.Gly4317Ser) rs567999404 0.00003
NM_005529.7(HSPG2):c.13037G>A (p.Gly4346Asp) rs748956430 0.00003
NM_005529.7(HSPG2):c.12682G>A (p.Glu4228Lys) rs138672955 0.00002
NM_005529.7(HSPG2):c.13138G>A (p.Ala4380Thr) rs779453903 0.00002
NM_005529.7(HSPG2):c.12676G>A (p.Val4226Met) rs760832004 0.00001
NM_005529.7(HSPG2):c.12688A>G (p.Ile4230Val) rs771043879 0.00001
NM_005529.7(HSPG2):c.12773A>G (p.Asp4258Gly) rs756568323 0.00001
NM_005529.7(HSPG2):c.12922C>T (p.Gln4308Ter) rs2097958823 0.00001
NM_005529.7(HSPG2):c.13000A>G (p.Ile4334Val) rs779443131 0.00001
NM_005529.7(HSPG2):c.13025C>T (p.Thr4342Met) rs772087950 0.00001
NM_005529.7(HSPG2):c.13034G>A (p.Gly4345Glu) rs1023997960 0.00001
NM_005529.7(HSPG2):c.13099G>A (p.Gly4367Ser) rs373820736 0.00001
NM_005529.7(HSPG2):c.13159C>T (p.Arg4387Cys) rs767431377 0.00001
NM_005529.7(HSPG2):c.12622G>A (p.Asp4208Asn)
NM_005529.7(HSPG2):c.12665+3G>A
NM_005529.7(HSPG2):c.12666-4G>A
NM_005529.7(HSPG2):c.12673G>A (p.Glu4225Lys) rs367606633
NM_005529.7(HSPG2):c.12676G>T (p.Val4226Leu)
NM_005529.7(HSPG2):c.12680C>T (p.Pro4227Leu)
NM_005529.7(HSPG2):c.12704G>A (p.Arg4235Gln)
NM_005529.7(HSPG2):c.12738G>A (p.Gln4246=)
NM_005529.7(HSPG2):c.12800G>A (p.Gly4267Glu)
NM_005529.7(HSPG2):c.12805C>A (p.Leu4269Ile)
NM_005529.7(HSPG2):c.12841C>T (p.Arg4281Cys)
NM_005529.7(HSPG2):c.12871G>A (p.Gly4291Ser)
NM_005529.7(HSPG2):c.12883C>T (p.Arg4295Trp)
NM_005529.7(HSPG2):c.12899G>A (p.Arg4300Gln)
NM_005529.7(HSPG2):c.12908G>A (p.Arg4303His)
NM_005529.7(HSPG2):c.12920T>C (p.Ile4307Thr)
NM_005529.7(HSPG2):c.12952C>T (p.Arg4318Trp) rs3736358
NM_005529.7(HSPG2):c.12958C>T (p.Pro4320Ser) rs772757002
NM_005529.7(HSPG2):c.12967A>T (p.Asn4323Tyr)
NM_005529.7(HSPG2):c.12988G>A (p.Gly4330Ser) rs769986876
NM_005529.7(HSPG2):c.12989G>A (p.Gly4330Asp)
NM_005529.7(HSPG2):c.12994G>T (p.Val4332Phe) rs1138469
NM_005529.7(HSPG2):c.13003G>A (p.Gly4335Ser)
NM_005529.7(HSPG2):c.13004-3C>G
NM_005529.7(HSPG2):c.13088C>G (p.Ser4363Trp)
NM_005529.7(HSPG2):c.13094G>A (p.Arg4365Gln) rs373773624
NM_005529.7(HSPG2):c.13094G>T (p.Arg4365Leu)
NM_005529.7(HSPG2):c.13109C>G (p.Pro4370Arg) rs886044123
NM_005529.7(HSPG2):c.13135C>T (p.Arg4379Cys)
NM_005529.7(HSPG2):c.13159C>A (p.Arg4387Ser) rs767431377

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