Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 5:35867437 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM056606

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB IL7R_353G_A_083010

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, is associated with 1 phenotype and is mentioned in 6 citations.

Variant displays