C2677565[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1031736	NM_007375.4(TARDBP):c.623G>A (p.Arg208Gln)	TARDBP (R208Q)	Single nucleotide variant (missense variant)	Amyotrophic lateral sclerosis type 10	GUncertain significance
Select item 21482	NM_007375.4(TARDBP):c.800A>G (p.Asn267Ser)	TARDBP	Single nucleotide variant (missense variant)	Amyotrophic lateral sclerosis type 10 +4 more	GConflicting classifications of pathogenicity