Original source

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

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58032726

This variation has 6 HGVS names - click the plus to show

14:g.22548589G>T
ENST00000613353.3:c.670+811G>T
ENST00000618259.3:c.667+811G>T
ENST00000611204.3:c.457+811G>T
ENST00000611116.1:c.273+811G>T
ENST00000616778.3:c.337+811G>T

Genotyping chips

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

About this variant

This variant overlaps 8 transcripts, has 3961 individual genotypes and is mentioned in 1 citation.

Variation displays