Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17472984, rs61163349

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni5

About this variant

This variant overlaps 14 transcripts and has 2845 sample genotypes.

Variant displays