Original source

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

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

Chromosome 16:3142454 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61457258

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 12 transcripts and has 1 individual genotype.

Variation displays