Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 2:9506861 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]

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

About this variant

This variant overlaps 3 transcripts and has 269 individual genotypes.

Variation displays