Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.22 (G)
Location

Chromosome 10:69382664 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs17850368, rs60876495

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 3806 sample genotypes and is mentioned in 4 citations.

Variant displays