Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.13 (T)
Location

Chromosome 1:231408555 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 3 HGVS names - click the plus to show

About this variant

Variant displays