ClinVar Miner

List of variants in gene RYR2 reported as likely benign for not provided

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Total variants: 111
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HGVS dbSNP
NC_000001.11:g.237042102G>C
NC_000001.11:g.237416750_237416755del
NM_001035.3(RYR2):c.10143-24C>T
NM_001035.3(RYR2):c.10381A>G (p.Met3461Val) rs147512481
NM_001035.3(RYR2):c.10495-218T>A
NM_001035.3(RYR2):c.10555-10T>C
NM_001035.3(RYR2):c.10690-301C>A
NM_001035.3(RYR2):c.10726-181G>A
NM_001035.3(RYR2):c.10839-283G>A
NM_001035.3(RYR2):c.10935+100A>G
NM_001035.3(RYR2):c.10936-108G>A
NM_001035.3(RYR2):c.10936-229A>G
NM_001035.3(RYR2):c.11092-11del rs397516499
NM_001035.3(RYR2):c.11246-158G>T
NM_001035.3(RYR2):c.1135G>A (p.Val379Met) rs199693714
NM_001035.3(RYR2):c.11476+60A>G
NM_001035.3(RYR2):c.11646+180G>C
NM_001035.3(RYR2):c.1171-14T>G
NM_001035.3(RYR2):c.11775+211A>G
NM_001035.3(RYR2):c.11775+310T>A
NM_001035.3(RYR2):c.11881-221C>T
NM_001035.3(RYR2):c.11881-270G>C
NM_001035.3(RYR2):c.11963-254T>C
NM_001035.3(RYR2):c.12159G>A (p.Glu4053=) rs41267517
NM_001035.3(RYR2):c.12842C>T (p.Thr4281Met) rs201829896
NM_001035.3(RYR2):c.12919C>T (p.Arg4307Cys) rs200092869
NM_001035.3(RYR2):c.1293-79G>A
NM_001035.3(RYR2):c.12957C>T (p.Val4319=) rs727504438
NM_001035.3(RYR2):c.13477-18A>G
NM_001035.3(RYR2):c.13477-206C>T
NM_001035.3(RYR2):c.1353C>T (p.Ser451=)
NM_001035.3(RYR2):c.13672C>T (p.His4558Tyr) rs773264033
NM_001035.3(RYR2):c.13740G>T (p.Thr4580=)
NM_001035.3(RYR2):c.14152-116T>A
NM_001035.3(RYR2):c.14152-274G>A
NM_001035.3(RYR2):c.14433+298G>A
NM_001035.3(RYR2):c.14656-105G>A
NM_001035.3(RYR2):c.14658C>G (p.Thr4886=)
NM_001035.3(RYR2):c.1479A>C (p.Gly493=)
NM_001035.3(RYR2):c.14896C>T (p.Leu4966=)
NM_001035.3(RYR2):c.1612+257A>T
NM_001035.3(RYR2):c.169-126G>A
NM_001035.3(RYR2):c.2389G>A (p.Gly797Arg) rs200121281
NM_001035.3(RYR2):c.2396+180C>G
NM_001035.3(RYR2):c.2613+188A>G
NM_001035.3(RYR2):c.2613+271C>T
NM_001035.3(RYR2):c.2613+89C>T
NM_001035.3(RYR2):c.2614-292T>G
NM_001035.3(RYR2):c.2614-294C>T
NM_001035.3(RYR2):c.2614-299A>G
NM_001035.3(RYR2):c.2614-304T>C
NM_001035.3(RYR2):c.2614-336A>G
NM_001035.3(RYR2):c.2718+159G>A
NM_001035.3(RYR2):c.2718+246G>C
NM_001035.3(RYR2):c.273+190T>C
NM_001035.3(RYR2):c.2823-177G>A
NM_001035.3(RYR2):c.294+14T>A
NM_001035.3(RYR2):c.295-107A>G
NM_001035.3(RYR2):c.3067-157G>C
NM_001035.3(RYR2):c.3067-287A>G
NM_001035.3(RYR2):c.309+138A>G
NM_001035.3(RYR2):c.3214+80G>T
NM_001035.3(RYR2):c.3380A>G (p.Glu1127Gly) rs200525962
NM_001035.3(RYR2):c.3407C>T (p.Ala1136Val) rs72549415
NM_001035.3(RYR2):c.3423+99A>T
NM_001035.3(RYR2):c.3598+265A>C
NM_001035.3(RYR2):c.4161-76A>G
NM_001035.3(RYR2):c.4182G>A (p.Lys1394=)
NM_001035.3(RYR2):c.4275+8G>C
NM_001035.3(RYR2):c.4445G>A (p.Arg1482His) rs373024059
NM_001035.3(RYR2):c.463+68C>T
NM_001035.3(RYR2):c.4683+190T>A
NM_001035.3(RYR2):c.4683+259T>C
NM_001035.3(RYR2):c.4684-215G>A
NM_001035.3(RYR2):c.5715+163T>C
NM_001035.3(RYR2):c.5716-143A>C
NM_001035.3(RYR2):c.5917-81G>A
NM_001035.3(RYR2):c.6336C>T (p.Ser2112=) rs373777614
NM_001035.3(RYR2):c.6440+229C>T
NM_001035.3(RYR2):c.6441-88A>G
NM_001035.3(RYR2):c.649A>G (p.Ile217Val) rs200642525
NM_001035.3(RYR2):c.6555+294A>G
NM_001035.3(RYR2):c.6555+322C>A
NM_001035.3(RYR2):c.6555+330G>A
NM_001035.3(RYR2):c.6555+331C>G
NM_001035.3(RYR2):c.6555+333C>T
NM_001035.3(RYR2):c.6688+229A>G
NM_001035.3(RYR2):c.6792+122G>A
NM_001035.3(RYR2):c.6793-195A>G
NM_001035.3(RYR2):c.7115+268G>A
NM_001035.3(RYR2):c.7115+289T>C
NM_001035.3(RYR2):c.7342+306C>T
NM_001035.3(RYR2):c.7342+42G>A
NM_001035.3(RYR2):c.773+141C>T
NM_001035.3(RYR2):c.7733+207A>G
NM_001035.3(RYR2):c.774-14G>T rs370114411
NM_001035.3(RYR2):c.774-296C>T
NM_001035.3(RYR2):c.7825-121T>A
NM_001035.3(RYR2):c.8129+210A>G
NM_001035.3(RYR2):c.8130-290T>C
NM_001035.3(RYR2):c.8145G>T (p.Glu2715Asp) rs200420897
NM_001035.3(RYR2):c.8590+124G>A
NM_001035.3(RYR2):c.8590+238G>A
NM_001035.3(RYR2):c.8714+125A>G
NM_001035.3(RYR2):c.8715-30G>A
NM_001035.3(RYR2):c.9067+277G>A
NM_001035.3(RYR2):c.9128+177G>T
NM_001035.3(RYR2):c.9128+263C>T
NM_001035.3(RYR2):c.9560A>G (p.Lys3187Arg) rs184218219
NM_001035.3(RYR2):c.9581-46C>T
NM_001035.3(RYR2):c.9655G>A (p.Val3219Met) rs371147744

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