Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome 1:201359243 (forward strand)|View in location tab

Co-located variant

COSMIC COSM209474

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 24 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 19 transcripts.

Variant displays