Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.35 (C)
Location

Chromosome 17:43091983 (forward strand) | View in location tab

Co-located

with COSMIC COSM148277 (T/C), COSM3755561 (T/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 23 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 25 transcripts, has 4476 individual genotypes, is associated with 3 phenotypes and is mentioned in 15 citations.

Variation displays