ClinVar Miner

List of variants in gene combination LOC126862019, TDP1 reported as benign for autosomal recessive disease

Included ClinVar conditions (1198):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_018319.4(TDP1):c.291A>G (p.Gln97=) rs3825663 0.25304
NM_018319.4(TDP1):c.400G>A (p.Ala134Thr) rs28365054 0.10566
NM_018319.4(TDP1):c.302C>T (p.Pro101Leu) rs35455108 0.00620

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