Variants in gene SPTB with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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_001355436.2(SPTB):c.4291C>T (p.Arg1431Ter)	rs757836263	0.00002
NM_001355436.2(SPTB):c.1249C>T (p.Gln417Ter)	rs2139606980
NM_001355436.2(SPTB):c.1A>G (p.Met1Val)	rs121918651
NM_001355436.2(SPTB):c.208C>T (p.Arg70Ter)	rs1566775577
NM_001355436.2(SPTB):c.2863C>T (p.Arg955Ter)	rs1555369657
NM_001355436.2(SPTB):c.3496C>T (p.Gln1166Ter)
NM_001355436.2(SPTB):c.3916C>T (p.Arg1306Ter)	rs150471537
NM_001355436.2(SPTB):c.4735C>T (p.Arg1579Ter)	rs760938057
NM_001355436.2(SPTB):c.4973+5G>A	rs1555367789
NM_001355436.2(SPTB):c.5856del (p.Ile1952fs)
NM_001355436.2(SPTB):c.6119_6120del (p.Thr2040fs)	rs2139480757
NM_001355436.2(SPTB):c.6224A>G (p.Glu2075Gly)	rs1235889026
NM_001355436.2(SPTB):c.647G>A (p.Arg216Gln)	rs1555371769

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