ClinVar Miner

List of variants in gene LOC129993163, MMAA studied for vitamin B deficiency

Included ClinVar conditions (24):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_172250.3(MMAA):c.-66+10G>C rs546775043 0.00165
NM_172250.3(MMAA):c.-69G>T rs886059086 0.00013
NM_172250.3(MMAA):c.-71G>C rs992491091 0.00003
NM_172250.3(MMAA):c.-68C>A rs886059087
NM_172250.3(MMAA):c.-68C>T rs886059087

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