Original source

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

Alleles
G/T|Ancestral: T|Ambiguity code: K|MAF: 0.25 (G)
Location

Chromosome 14:22548589 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58032726

HGVS names

This variant has 3 HGVS names - Hide

14:g.22548589G>T
ENST00000611116.1:c.273+811G>T
ENST00000616778.4:c.337+811G>T

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 3961 sample genotypes and is mentioned in 1 citation.

Variant displays