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: 0.24 (G)
Location

Chromosome 14:22533736 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1753443, rs57770305

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

14:g.22533736G>T
ENST00000613353.1:c.398-13770G>T
ENST00000618259.1:c.395-13770G>T
ENST00000616778.1:c.65-13770G>T
ENST00000611204.1:c.185-13770G>T

This variation has assays on 5 chips - click the plus to show

Variation displays