Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.01 (C)
Location

Chromosome 15:40694071 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs36229879

This variant has 4 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

Variant displays