Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 5 HGVS names - click the plus to show

14:g.22530666G>T
ENST00000613353.4:c.398-16840G>T
ENST00000618259.4:c.394+16668G>T
ENST00000616778.4:c.65-16840G>T
ENST00000611204.4:c.185-16840G>T

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 13 transcripts, has 3960 sample genotypes and is mentioned in 1 citation.

Variant displays