Original source

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

G/A/C | Ancestral: A | Ambiguity code: V | MAF: 0.43 (A)

Chromosome 17:31352228 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 20 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 20 transcripts, has 3943 sample genotypes and is mentioned in 1 citation.

Variant displays