Original source

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

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

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

Co-located variants

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

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB 3503, 2010_April_001_027_IL7R_146661_0004

HGVS names

This variant has 12 HGVS names - Show

About this variant

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

Variant displays