Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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