Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.45 (T)
Location

Chromosome 10:99533584 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57597073

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 3 transcripts and has 2511 sample genotypes.

Variant displays