List of variants in gene SPTAN1 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001130438.3(SPTAN1):c.7234G>A (p.Glu2412Lys)	rs1336849921	0.00002
NM_001130438.3(SPTAN1):c.7316C>T (p.Thr2439Ile)	rs746532292	0.00002
NM_001130438.3(SPTAN1):c.2617G>A (p.Glu873Lys)	rs776279771	0.00001
NM_001130438.3(SPTAN1):c.2197C>T (p.Arg733Ter)	rs1852298912
NM_001130438.3(SPTAN1):c.2612del (p.Lys871fs)	rs1852530020
NM_001130438.3(SPTAN1):c.2815C>T (p.Leu939Phe)	rs1852827656
NM_001130438.3(SPTAN1):c.4455A>C (p.Lys1485Asn)	rs1856146384
NM_001130438.3(SPTAN1):c.4561G>T (p.Asp1521Tyr)
NM_001130438.3(SPTAN1):c.6611G>A (p.Arg2204Gln)	rs1858936991
NM_001130438.3(SPTAN1):c.74G>A (p.Arg25Gln)	rs1850091477

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