List of variants in gene MMACHC, PRDX1 studied for vitamin B12 deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_181697.3(PRDX1):c.515-1G>T	rs751828470	0.00004
GRCh37/hg19 1p34.1(chr1:45965972-45979054)
NC_000001.10:g.(?_45966005)_(45977106_?)dup
NC_000001.10:g.(?_45973008)_(45977106_?)del
NM_181697.3(PRDX1):c.515-2A>T	rs1379672870

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