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
ENST00000613353.3:c.398-13770G>T
ENST00000618259.3:c.395-13770G>T
ENST00000616778.3:c.65-13770G>T
ENST00000611204.3:c.185-13770G>T

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 13 transcripts, has 2560 individual genotypes, is associated with 3 phenotypes and is mentioned in 9 citations.

Variation displays