Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.08 (T)
Location

Chromosome 16:50781521 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17314306

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 13 transcripts, 1 regulatory feature, has 2846 sample genotypes and is mentioned in 1 citation.

Variant displays