Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)

Chromosome 19:33299848 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status


Archive dbSNP rs386583145

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 5 transcripts and has 2675 sample genotypes.

Variant displays