Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.10 (G)
Location

Chromosome 2:118848857 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

2:g.118848857C>G

About this variant

This variant overlaps 2 transcripts and has 2508 sample genotypes.

Variant displays