Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.17 (T)
Location

Chromosome 12:53721035 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs4445683, rs57482662

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 21 transcripts and has 2772 sample genotypes.

Variant displays