Original source

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