Original source

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

Alleles
A/G|Ambiguity code: R|MAF: 0.27 (A)
Location

Chromosome 17:27765605 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms
HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, has 2605 sample genotypes and is mentioned in 2 citations.

Variant displays