Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.22 (C)
Location

Chromosome 9:95183514 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

Variant displays