Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 5:35873593 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM983406 ; PhenCode IL7Rbase_D0050:g.17639G>A (G/A)

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 3503, 2010_April_001_027_IL7R_146661_0004

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and is associated with 2 phenotypes.

Variant displays