Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.42 (T)
Location

Chromosome 12:124836304 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56888601

This variant has 10 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 3694 sample genotypes, is associated with 1 phenotype and is mentioned in 8 citations.

Variant displays