Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.10 (G)

Chromosome 2:47164910 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs1693875, rs56850384

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 10 transcripts, has 4036 sample genotypes and is mentioned in 1 citation.

Variant displays