Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.03 (T)
Location

Chromosome 12:49263403 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 6 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 3408 sample genotypes.

Variant displays