Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 9:121268842 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 11 transcripts and has 267 individual genotypes.

Variation displays