Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.24 (T)
Location

Chromosome 9:81690785 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61167013

This variant has 2 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

Variant displays