Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 5:35873695 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 3503, 2010_April_001_027_IL7R_146661_0004

This variation has 14 HGVS names - click the plus to show

Variation displays