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 16:88646828 (forward strand) | View in location tab

Co-located

with COSMIC COSM3755197 (A/G) ; HGMD-PUBLIC CM983302

Most severe consequence
Evidence status

Clinical significance

This variation has 11 synonyms - click the plus to show

This variation has 17 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 11 transcripts, has 4097 individual genotypes, is associated with 2 phenotypes and is mentioned in 26 citations.

Variation displays