Original source

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

Alleles
G/T|Ancestral: T|Ambiguity code: K|MAF: 0.28 (G)
Location

Chromosome 14:22530666 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58628743

HGVS names

This variant has 2 HGVS names - Hide

14:g.22530666G>T
ENST00000616778.4:c.65-16840G>T

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 10 transcripts, has 3960 sample genotypes and is mentioned in 1 citation.

Variant displays