Related gene-specific medical variations for Gene (Select 51561) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2591948	NM_016584.3(IL23A):c.317C>T (p.Ser106Leu)	IL23A, LOC132090128 (S106L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221371	NM_016584.3(IL23A):c.337C>G (p.Pro113Ala)	IL23A, LOC132090128 (P113A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 403490	NC_000012.12:g.56339747G>A	LOC132090128, STAT2 +1 more	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign

Format

Sort by

Choose Destination