Original source

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

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 28 transcripts and has 2506 sample genotypes.

Variant displays