Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 5:35871070 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002997 ; PhenCode IL7Rbase_D0050:g.15116C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 3504, 2010_April_001_028_IL7R_146661_0005

This variation has 10 HGVS names - click the plus to show

Variation displays