Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.32 (T)
Location

Chromosome 1:109558291 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60808626

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

About this variant

This variant overlaps 1 transcript and has 2512 sample genotypes.

Variant displays