Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.34 (A)
Location

Chromosome 20:761203 (forward strand) | View in location tab

Co-located

with COSMIC COSM3758788 (A/G)

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 3801 individual genotypes.

Variation displays