ClinVar Miner

List of variants in gene ACD reported as benign for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_001082486.1(ACD):c.162C>T (p.Pro54=) rs73597595
NM_001082486.2(ACD):c.1207-10C>T rs67185288
NM_001082486.2(ACD):c.132C>T (p.Gly44=) rs138527794
NM_001082486.2(ACD):c.1371G>T (p.Pro457=) rs14920
NM_001082486.2(ACD):c.444C>T (p.Leu148=) rs151132164
NM_001082486.2(ACD):c.801C>T (p.Ala267=) rs72549181
NM_001082486.2(ACD):c.80G>A (p.Arg27Gln) rs142507451
NM_001082486.2(ACD):c.819C>T (p.Pro273=) rs138740815
NM_001082486.2(ACD):c.923G>A (p.Gly308Glu) rs147189192

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