Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.46 (A)
Location

Chromosome 9:73167594 (forward strand)|View in location tab

Co-located variant

dbSNP rs758692597 (G/-)

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms
HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 6 transcripts and has 4306 sample genotypes.

Variant displays