Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - 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 9 citations.

Variant displays