Original source

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

A/C/G | Ancestral: A | Ambiguity code: V | MAF: < 0.01 (G)

Chromosome 1:167282448 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs58160005

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 20 transcripts and has 2775 sample genotypes.

Variant displays