ClinVar Miner

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

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_015702.2(MMADHC):c.412G>A (p.Glu138Lys) rs61746421
NM_015702.2(MMADHC):c.428G>T (p.Ser143Ile) rs34886916
NM_015702.2(MMADHC):c.453G>A (p.Gln151=) rs11545261
NM_015702.2(MMADHC):c.478+6T>G rs13402787
NM_015702.2(MMADHC):c.87A>C (p.Lys29Asn) rs61750442

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