Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.16 (G)
Location

Chromosome 9:730054 (forward strand) | View in location tab

Co-located

with COSMIC COSM150571 (A/G)

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 3907 individual genotypes.

Variation displays