Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.45 (G)
Location

Chromosome 9:21816529 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17760747, rs58101861

HGVS names

This variant has 9 HGVS names - Hide

9:g.21816529A>G
ENST00000419385.5:c.146-185A>G
ENST00000580900.5:c.121-185A>G
ENST00000579422.5:n.509-185A>G
ENST00000404796.2:c.121-185A>G
ENST00000380172.8:c.121-185A>G
ENST00000460874.6:c.172-185A>G
ENST00000580718.1:c.121-185A>G
ENST00000427788.2:n.507-185A>G

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 10 transcripts, has 4034 sample genotypes, is associated with 2 phenotypes and is mentioned in 8 citations.

Variant displays