Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.11 (A)
Location

Chromosome 15:67154493 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60888448, rs56470392

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 9 transcripts, has 3692 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays