Original source

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

Alleles
T/A | Ambiguity code: W | MAF: 0.36 (T)
Location

Chromosome 11:17074603 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17472984, rs61163349

This variant has 7 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni5

About this variant

This variant overlaps 14 transcripts and has 2556 sample genotypes.

Variant displays