ClinVar Miner

List of variants in gene ADGRV1 reported as uncertain significance for Febrile seizures, familial, 4

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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_032119.4(ADGRV1):c.6133G>A (p.Gly2045Arg) rs41308846 0.00484
NM_032119.4(ADGRV1):c.18273A>G (p.Ala6091=) rs137853918 0.00316
NM_032119.4(ADGRV1):c.3151G>T (p.Asp1051Tyr) rs145556097 0.00195
NM_032119.4(ADGRV1):c.3191A>C (p.Glu1064Ala) rs190922596 0.00195
NM_032119.4(ADGRV1):c.1855T>G (p.Leu619Val) rs202064612 0.00083
NM_032119.4(ADGRV1):c.8469T>G (p.His2823Gln) rs188452841 0.00039
NM_032119.4(ADGRV1):c.14959G>A (p.Gly4987Arg) rs190988309 0.00034
NM_032119.4(ADGRV1):c.7468G>A (p.Ala2490Thr) rs143632883 0.00025
NM_032119.4(ADGRV1):c.2456G>A (p.Ser819Asn) rs182395524 0.00014
NM_032119.4(ADGRV1):c.11338C>T (p.Arg3780Cys) rs201742794 0.00011
NM_032119.4(ADGRV1):c.12032G>T (p.Gly4011Val) rs369044000 0.00001
NM_032119.4(ADGRV1):c.259A>G (p.Ile87Val) rs1763564700 0.00001
NM_032119.4(ADGRV1):c.323C>G (p.Pro108Arg) rs1158908533 0.00001
NM_032119.4(ADGRV1):c.10195C>T (p.His3399Tyr)
NM_032119.4(ADGRV1):c.11585A>G (p.Asp3862Gly) rs2149981215
NM_032119.4(ADGRV1):c.14602A>G (p.Ile4868Val) rs1561765715
NM_032119.4(ADGRV1):c.15185A>T (p.Glu5062Val)
NM_032119.4(ADGRV1):c.15212A>G (p.Glu5071Gly) rs1762337320
NM_032119.4(ADGRV1):c.15415G>C (p.Glu5139Gln) rs776241274
NM_032119.4(ADGRV1):c.17371A>G (p.Thr5791Ala)
NM_032119.4(ADGRV1):c.22+25188A>C rs1758425024
NM_032119.4(ADGRV1):c.263C>T (p.Pro88Leu)
NM_032119.4(ADGRV1):c.4205C>T (p.Thr1402Ile)
NM_032119.4(ADGRV1):c.6556C>G (p.Pro2186Ala) rs1357549892
NM_032119.4(ADGRV1):c.7135G>A (p.Gly2379Arg) rs549050123
NM_032119.4(ADGRV1):c.7413C>A (p.Ser2471Arg) rs746779681
NM_032119.4(ADGRV1):c.8471G>T (p.Gly2824Val) rs975296721
NM_032119.4(ADGRV1):c.9163G>C (p.Glu3055Gln)

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