Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.18 (C)
Location

Chromosome 6:13240912 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61328368

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

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_Human660W-quad

About this variant

This variant overlaps 3 transcripts and has 2508 sample genotypes.

Variant displays