Original source

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

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

Chromosome 19:8975282 (forward strand) | View in location tab

Co-located

with COSMIC COSM4132888 (A/G), COSM4132887 (A/G)

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 4038 individual genotypes.

Variation displays