ClinVar Miner

List of variants reported as likely benign for methionine adenosyltransferase deficiency by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_000429.3(MAT1A):c.*1092C>G rs41284062
NM_000429.3(MAT1A):c.*1292G>C rs58141836
NM_000429.3(MAT1A):c.*299G>A rs7097297
NM_000429.3(MAT1A):c.*529G>A rs10509413
NM_000429.3(MAT1A):c.*569C>G rs78720701
NM_000429.3(MAT1A):c.*863G>A rs41284064
NM_000429.3(MAT1A):c.-153C>T rs11595587
NM_000429.3(MAT1A):c.-73_-72insGAAAAA rs145126070

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