Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.01 (G)
Location

Chromosome 14:104769303 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

This variant has 2 HGVS names - click the plus to show

About this variant

Variant displays