Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 1:169477478 (forward strand) | View in location tab

Co-located

with COSMIC COSM3802763 (G/A) ; HGMD-PUBLIC CM991264

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_252_SLC19A2_603941_0001, 12261

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and is associated with 2 phenotypes.

Variant displays