Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 12:43762040 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 15 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 21 transcripts and has 49 sample genotypes.

Variant displays