Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.07 (C)
Location

Chromosome 12:21642359 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56759406

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2512 sample genotypes.

Variant displays