Original source

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

Alleles
C/G|Ancestral: G|Ambiguity code: S|MAF: 0.29 (C)
Location

Chromosome 2:118078449 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR062118

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs61203538

HGVS name

2:g.118078449C>G

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant has 4352 sample genotypes and is mentioned in 104 citations.

Variant displays