Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.34 (A)
Location

Chromosome 15:24990569 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56619905, rs12913018

HGVS names

This variant has 5 HGVS names - Hide

15:g.24990569G>A
ENST00000557230.1:c.*400-8401G>A
ENST00000551631.6:n.888-7797G>A
ENST00000551312.6:c.*953+8132G>A
ENST00000551361.1:n.444+8132G>A

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 7 transcripts and has 3684 sample genotypes.

Variant displays