Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.40 (A)
Location

Chromosome 6:41069249 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms
HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 19 transcripts and has 5941 sample genotypes.

Variant displays