Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.26 (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
ENST00000613353.1:c.670+811G>T
ENST00000618259.1:c.667+811G>T
ENST00000611204.1:c.457+811G>T
ENST00000616778.1:c.337+811G>T
ENST00000611116.1:c.273+811G>T

Genotyping chips

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

Variation displays