Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.23 (A)
Location

Chromosome 2:27136359 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

2:g.27136359C>A

About this variant

This variant overlaps 11 transcripts and has 2508 sample genotypes.

Variant displays