ClinVar Miner

List of variants in gene ADGRV1 reported as benign by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP
NM_032119.4(ADGRV1):c.-98G>A
NM_032119.4(ADGRV1):c.10039T>C (p.Phe3347Leu) rs10067636
NM_032119.4(ADGRV1):c.10126A>G (p.Ile3376Val) rs200528472
NM_032119.4(ADGRV1):c.10411G>A (p.Glu3471Lys) rs2366928
NM_032119.4(ADGRV1):c.10577T>C (p.Met3526Thr) rs41311343
NM_032119.4(ADGRV1):c.1086A>G (p.Leu362=) rs186639101
NM_032119.4(ADGRV1):c.10936T>C (p.Ser3646Pro) rs13171868
NM_032119.4(ADGRV1):c.11581-3dup rs34894132
NM_032119.4(ADGRV1):c.11599G>A (p.Glu3867Lys) rs10062026
NM_032119.4(ADGRV1):c.11682C>T (p.Pro3894=) rs2438349
NM_032119.4(ADGRV1):c.13654-5C>T rs367554300
NM_032119.4(ADGRV1):c.14309G>A (p.Arg4770His) rs41304892
NM_032119.4(ADGRV1):c.14515C>G (p.Gln4839Glu) rs79464236
NM_032119.4(ADGRV1):c.14654A>G (p.Asn4885Ser) rs61731030
NM_032119.4(ADGRV1):c.15343C>T (p.Leu5115=) rs41304886
NM_032119.4(ADGRV1):c.16031A>G (p.Glu5344Gly) rs2438374
NM_032119.4(ADGRV1):c.16279G>A (p.Val5427Met) rs2438378
NM_032119.4(ADGRV1):c.17017A>G (p.Lys5673Glu) rs41303350
NM_032119.4(ADGRV1):c.17626G>A (p.Val5876Ile) rs2247870
NM_032119.4(ADGRV1):c.17735C>G (p.Ser5912Cys) rs146120983
NM_032119.4(ADGRV1):c.18273A>G (p.Ala6091=) rs137853918
NM_032119.4(ADGRV1):c.18311-9dup rs140911567
NM_032119.4(ADGRV1):c.18433-5del rs35858094
NM_032119.4(ADGRV1):c.18475A>G (p.Met6159Val) rs77469944
NM_032119.4(ADGRV1):c.2367+8C>T rs2366773
NM_032119.4(ADGRV1):c.2553+11T>A rs73181640
NM_032119.4(ADGRV1):c.3279G>T (p.Leu1093Phe) rs2366777
NM_032119.4(ADGRV1):c.3295A>G (p.Thr1099Ala) rs61754947
NM_032119.4(ADGRV1):c.3303A>G (p.Val1101=) rs80069610
NM_032119.4(ADGRV1):c.4254T>C (p.Tyr1418=) rs149459739
NM_032119.4(ADGRV1):c.4939A>G (p.Ile1647Val) rs72782753
NM_032119.4(ADGRV1):c.5525-7C>T rs137853919
NM_032119.4(ADGRV1):c.5830G>A (p.Asp1944Asn) rs41302834
NM_032119.4(ADGRV1):c.5851G>A (p.Val1951Ile) rs4916684
NM_032119.4(ADGRV1):c.5953A>G (p.Asn1985Asp) rs41303352
NM_032119.4(ADGRV1):c.5960C>T (p.Pro1987Leu) rs4916685
NM_032119.4(ADGRV1):c.6012G>T (p.Leu2004Phe) rs16868972
NM_032119.4(ADGRV1):c.6095C>T (p.Ala2032Val) rs142013761
NM_032119.4(ADGRV1):c.6133G>A (p.Gly2045Arg) rs41308846
NM_032119.4(ADGRV1):c.6289C>T (p.Arg2097Cys) rs16868974
NM_032119.4(ADGRV1):c.6317C>T (p.Ala2106Val) rs186999408
NM_032119.4(ADGRV1):c.6318G>A (p.Ala2106=) rs190981860
NM_032119.4(ADGRV1):c.6608T>C (p.Val2203Ala) rs200055351
NM_032119.4(ADGRV1):c.7284T>C (p.Asn2428=) rs148932387
NM_032119.4(ADGRV1):c.746G>A (p.Arg249Lys) rs41303344
NM_032119.4(ADGRV1):c.7582C>T (p.Pro2528Ser) rs201733037
NM_032119.4(ADGRV1):c.8133C>T (p.Ser2711=) rs116446814
NM_032119.4(ADGRV1):c.8730+9C>T rs886043931
NM_032119.4(ADGRV1):c.9366A>G (p.Thr3122=) rs200412477
NM_032119.4(ADGRV1):c.9927T>G (p.Pro3309=) rs16869042

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