Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.15 (G)
Location

Chromosome 9:73160319 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms
HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 7 transcripts and has 3691 sample genotypes.

Variant displays