Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.03 (G)
Location

Chromosome 2:208121117 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

2:g.208121117C>G

About this variant

This variant overlaps 1 transcript and has 2834 sample genotypes.

Variant displays