Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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