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: 0.29 (G)
Location

Chromosome 14:22530666 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58628743

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

14:g.22530666G>T
ENST00000613353.1:c.398-16840G>T
ENST00000618259.1:c.394+16668G>T
ENST00000616778.1:c.65-16840G>T
ENST00000611204.1:c.185-16840G>T

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

Variation displays