Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.13 (C)
Location

Chromosome 6:43519625 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 28 transcripts and has 2506 sample genotypes.

Variant displays