ClinVar Miner

List of variants in gene combination LOC126807124, MTTP reported as benign for abetalipoproteinemia

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000253.3(MTTP):c.-241G>A	rs11944752	0.26041
NM_000253.3(MTTP):c.-252G>C	rs11944749	0.15525

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