Original source

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

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

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

Co-located

with dbSNP rs199731828 (G/A/T)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2514 sample genotypes.

Variant displays