Variants in gene VPS13B with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 13

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HGVS	dbSNP	gnomAD frequency
NM_152564.5(VPS13B):c.7708G>A (p.Asp2570Asn)	rs140179844	0.00117
NM_152564.5(VPS13B):c.5803T>G (p.Ser1935Ala)	rs138930771	0.00053
NM_017890.5(VPS13B):c.4186C>T (p.Gln1396Ter)	rs559590419	0.00001
NM_152564.5(VPS13B):c.5220G>T (p.Glu1740Asp)	rs780598553	0.00001
NM_152564.5(VPS13B):c.6947A>G (p.Tyr2316Cys)	rs386834104	0.00001
NM_152564.5(VPS13B):c.7051-1G>A	rs930144563	0.00001
NM_017890.5(VPS13B):c.4289dup (p.Phe1431fs)	rs1427643616
NM_152564.5(VPS13B):c.11673_11674del (p.Ala3892fs)	rs1180933570
NM_152564.5(VPS13B):c.11750_11752dup (p.Asp3917dup)	rs386834068
NM_152564.5(VPS13B):c.3240del (p.Pro1081fs)	rs764544747
NM_152564.5(VPS13B):c.3G>A (p.Met1Ile)	rs1060499779
NM_152564.5(VPS13B):c.5908+2dup	rs587777381
NM_152564.5(VPS13B):c.9331-1G>T	rs386834119

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