Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 5:35873559 (forward strand) | View in location tab

Co-located

with COSMIC COSM1695579 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB IL7R_617G_A_031511

This variation has 24 HGVS names - click the plus to show

Variation displays