This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C/G/T | Ancestral: A | Ambiguity code: N | MAF: 0.12 (C)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58160005

This variation has 33 HGVS names - click the plus to show

About this variant

This variant overlaps 30 transcripts and has 2775 individual genotypes.

Variation displays