Variants in gene SALL1 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_002968.3(SALL1):c.411C>T (p.Ser137=)	rs151051011	0.00093
NM_002968.3(SALL1):c.3750C>T (p.Asn1250=)	rs142653419	0.00023
NM_002968.3(SALL1):c.2373C>A (p.Gly791=)	rs377295510	0.00009
NM_002968.3(SALL1):c.1738A>G (p.Ile580Val)	rs761575154	0.00008
NM_002968.3(SALL1):c.3270C>T (p.Asn1090=)	rs143637930	0.00007
NM_002968.3(SALL1):c.1715C>T (p.Thr572Met)	rs373471563	0.00006
NM_002968.3(SALL1):c.220G>A (p.Val74Ile)	rs529479120	0.00001
NM_002968.3(SALL1):c.2590G>A (p.Ala864Thr)	rs199626036	0.00001
NM_002968.3(SALL1):c.2825C>A (p.Pro942His)	rs751069468	0.00001
NM_002968.2(SALL1):c.466_477dup (p.Ser159_Gly160insSerSerSerSer)	rs113614842

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