Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.42 (C)
Location

Chromosome 22:37239850 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts and has 2528 sample genotypes.

Variant displays