Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/G/T | Ancestral: C | Ambiguity code: B | MAF: 0.33 (C)

Chromosome 14:102134513 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs58353414

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2511 sample genotypes.

Variant displays