Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: < 0.01 (G)
Location

Chromosome 9:81690731 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386455073

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

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

Variant displays