Original source

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

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

Chromosome 2:208125316 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

2:g.208125316C>A

About this variant

This variant overlaps 2 transcripts and has 2505 sample genotypes.

Variant displays