Original source

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

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

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

Co-located

with HGMD-PUBLIC CM056606

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB IL7R_353G_A_083010

This variation has 13 HGVS names - click the plus to show

Variation displays