ClinVar Miner

List of variants in gene combination ADAR, LOC126805874 reported as likely benign for autosomal recessive disease

Included ClinVar conditions (1198):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_001111.5(ADAR):c.2553C>T (p.Cys851=) rs138927668 0.00304
NM_001111.5(ADAR):c.2598C>G (p.Arg866=) rs749389266 0.00004
NM_001111.5(ADAR):c.2649C>T (p.Val883=) rs200989942 0.00004
NM_001111.5(ADAR):c.2762+10G>A rs879809934 0.00004
NM_001111.5(ADAR):c.2592C>T (p.Leu864=) rs138707431 0.00002
NM_001111.5(ADAR):c.2762+7G>A rs201315688 0.00002
NM_001111.5(ADAR):c.2610C>T (p.Ala870=) rs777928382 0.00001
NM_001111.5(ADAR):c.2659T>C (p.Leu887=) rs759505132 0.00001
NM_001111.5(ADAR):c.2668+11C>T rs768855853 0.00001
NM_001111.5(ADAR):c.2669-12A>T rs1696978630 0.00001
NM_001111.5(ADAR):c.2669-9C>T rs777184958 0.00001
NM_001111.5(ADAR):c.2762+18T>C rs775859361 0.00001
NM_001111.5(ADAR):c.2565G>A (p.Leu855=)
NM_001111.5(ADAR):c.2565G>T (p.Leu855=) rs2101585659
NM_001111.5(ADAR):c.2592C>G (p.Leu864=) rs138707431
NM_001111.5(ADAR):c.2607G>T (p.Leu869=)
NM_001111.5(ADAR):c.2610C>A (p.Ala870=)
NM_001111.5(ADAR):c.2625A>G (p.Lys875=) rs2101585294
NM_001111.5(ADAR):c.2646T>A (p.Gly882=)
NM_001111.5(ADAR):c.2652C>T (p.Val884=)
NM_001111.5(ADAR):c.2661G>A (p.Leu887=)
NM_001111.5(ADAR):c.2668+10G>A rs2101584941
NM_001111.5(ADAR):c.2668+13C>T
NM_001111.5(ADAR):c.2668+15G>A
NM_001111.5(ADAR):c.2668+18A>G
NM_001111.5(ADAR):c.2668+19C>T rs2101584874
NM_001111.5(ADAR):c.2668+20A>G
NM_001111.5(ADAR):c.2669-11C>T
NM_001111.5(ADAR):c.2669-19G>A
NM_001111.5(ADAR):c.2669-5C>T
NM_001111.5(ADAR):c.2669-8C>T rs755765435
NM_001111.5(ADAR):c.2670G>A (p.Gly890=)
NM_001111.5(ADAR):c.2676C>T (p.Arg892=)
NM_001111.5(ADAR):c.2721T>C (p.Asn907=)
NM_001111.5(ADAR):c.2730T>C (p.His910=)
NM_001111.5(ADAR):c.2751A>G (p.Arg917=)
NM_001111.5(ADAR):c.2763-27_2763-14del

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