Original source

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

Alleles
G/T|Ancestral: T|Ambiguity code: K|MAF: 0.22 (G)
Location

Chromosome 14:22533736 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1753443, rs57770305

HGVS names

This variant has 2 HGVS names - Hide

14:g.22533736G>T
ENST00000616778.4:c.65-13770G>T

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 3965 sample genotypes, is associated with 3 phenotypes and is mentioned in 9 citations.

Variant displays