Original source

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

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

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

Most severe consequence
Synonymous variant
Evidence status

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