List of variants in gene LRPPRC reported as uncertain significance for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_133259.4(LRPPRC):c.4132A>G (p.Ser1378Gly)	rs149693840	0.00024
NM_133259.4(LRPPRC):c.4128del (p.Glu1377fs)	rs759052246	0.00010
NM_133259.4(LRPPRC):c.2210+4A>C	rs190007694	0.00009
NM_133259.4(LRPPRC):c.3430C>T (p.Arg1144Cys)	rs760016065	0.00009
NM_133259.4(LRPPRC):c.4056T>A (p.Asp1352Glu)	rs146630100	0.00007
NM_133259.4(LRPPRC):c.124G>A (p.Ala42Thr)	rs752575254	0.00003
NM_133259.4(LRPPRC):c.3350G>A (p.Arg1117Gln)	rs369972045	0.00002
NM_133259.4(LRPPRC):c.2398G>A (p.Gly800Ser)	rs747400412	0.00001
NC_000002.11:g.(?_44113362)_(44223145_?)dup
NM_133259.4(LRPPRC):c.110CCT[1] (p.Ser38del)	rs863224061
NM_133259.4(LRPPRC):c.1253A>C (p.Asn418Thr)	rs373908553
NM_133259.4(LRPPRC):c.134C>G (p.Ala45Gly)	rs2103796814
NM_133259.4(LRPPRC):c.2741C>A (p.Pro914Gln)	rs1463658772
NM_133259.4(LRPPRC):c.2966G>A (p.Arg989His)	rs774857058

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