List of variants in gene NIPBL reported as uncertain significance by Institute of Human Genetics, University of Leipzig Medical Center

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_133433.4(NIPBL):c.7552G>A (p.Asp2518Asn)	rs961989627	0.00001
NM_133433.4(NIPBL):c.1285C>G (p.Leu429Val)	rs1743429461
NM_133433.4(NIPBL):c.1717T>C (p.Cys573Arg)	rs1744567400
NM_133433.4(NIPBL):c.1925C>T (p.Thr642Ile)	rs1744597297
NM_133433.4(NIPBL):c.3527A>G (p.Glu1176Gly)	rs1275880743
NM_133433.4(NIPBL):c.3928G>A (p.Ala1310Thr)	rs2149676816
NM_133433.4(NIPBL):c.8370del (p.Thr2791fs)	rs1755229121

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