Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.24 (C)
Location

Chromosome 13:33022117 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs560427

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

About this variant

This variant overlaps 2 transcripts and has 2508 sample genotypes.

Variant displays