List of variants in gene SLFN13 studied for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_144682.6(SLFN13):c.1974A>C (p.Lys658Asn)	rs75812929	0.10992
NM_144682.6(SLFN13):c.704C>T (p.Ser235Phe)	rs72483216	0.03376
NM_144682.6(SLFN13):c.1494A>G (p.Leu498=)	rs112473055	0.00600
NM_144682.6(SLFN13):c.454G>A (p.Asp152Asn)	rs115889903	0.00568
NM_144682.6(SLFN13):c.2616A>G (p.Thr872=)	rs140062622	0.00312
NM_144682.6(SLFN13):c.1515C>T (p.Thr505=)
NM_144682.6(SLFN13):c.1677C>T (p.Leu559=)	rs764700107

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