Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.42 (G)
Location

Chromosome 11:17498195 (forward strand) | View in location tab

Co-located

with COSMIC COSM3736035 (C/G), COSM3736036 (C/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

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

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2590 individual genotypes.

Variation displays