ClinVar Miner

List of variants in gene RTTN reported as benign for bone disorder

Included ClinVar conditions (1346):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_173630.4(RTTN):c.842-30A>G rs283250 0.94865
NM_173630.4(RTTN):c.2482-24T>G rs11665653 0.80619
NM_173630.4(RTTN):c.5282T>C (p.Phe1761Ser) rs4891392 0.79319
NM_173630.4(RTTN):c.376T>G (p.Ser126Ala) rs3911730 0.73528
NM_173630.4(RTTN):c.4653+25C>T rs1369292 0.73057
NM_173630.4(RTTN):c.6144A>G (p.Val2048=) rs2304378 0.16509
NM_173630.4(RTTN):c.2886-9A>G rs75225724 0.01465
NM_173630.4(RTTN):c.4375-24C>T rs285228
NM_173630.4(RTTN):c.725_727dup (p.Gly242dup) rs58913700

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