List of variants in gene LRPPRC reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_133259.4(LRPPRC):c.1426A>G (p.Thr476Ala)	rs115507225	0.00066
NM_133259.4(LRPPRC):c.1678A>T (p.Ile560Leu)	rs144826521	0.00058
NM_133259.4(LRPPRC):c.802G>C (p.Asp268His)	rs756849117	0.00007
NC_000002.12:g.43996149G>A
NM_133259.4(LRPPRC):c.1936G>T (p.Val646Phe)	rs752968314
NM_133259.4(LRPPRC):c.254G>C (p.Trp85Ser)	rs1453934366
NM_133259.4(LRPPRC):c.3279G>A (p.Ala1093=)
NM_133259.4(LRPPRC):c.3323G>T (p.Ser1108Ile)	rs1572900944
NM_133259.4(LRPPRC):c.3342A>G (p.Gln1114=)	rs1572900912

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