Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)
Location

Chromosome 11:32387514 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17480633

This variation has 2 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts and has 2556 individual genotypes.

Variation displays