Original source

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

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

Chromosome 9:37429817 (forward strand) | View in location tab


with COSMIC COSM4163856 (A/G), COSM4163857 (A/G)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 9 synonyms - Show

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 13 transcripts, has 3803 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays