Original source

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

Alleles
T/A|Ancestral: A|Ambiguity code: W|MAF: 0.23 (A)
Location

Chromosome 14:20473254 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17879951, rs17883835

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 10 transcripts and has 3901 sample genotypes.

Variant displays