Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.45 (T)
Location

Chromosome 15:88855374 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs52808766, rs59582752

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 7 transcripts and has 3841 sample genotypes.

Variant displays