Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.40 (C)
Location

Chromosome 12:6535615 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56744165

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

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 28 transcripts, 1 regulatory feature, has 4009 sample genotypes and is mentioned in 3 citations.

Variant displays