Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.27 (A)
Location

Chromosome 9:99146633 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CS045221

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58752737, rs57667361

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 6 transcripts, has 4398 sample genotypes and is mentioned in 7 citations.

Variant displays