Original source

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

Alleles
G/-|Ancestral: G|MAF: 0.35 (G)
Location

Chromosome 6:166159960 (forward strand)|View in location tab

Co-located variant

dbSNP rs199731828 (G/A/T)

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2514 sample genotypes.

Variant displays