Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/C|Ambiguity code: Y
Location

Chromosome 16:2617854 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 6 transcripts and 1 regulatory feature.

Variant displays