Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.41 (G)
Location

Chromosome 17:82209113 (forward strand)|View in location tab

Co-located variant

dbSNP rs533761551 (G/T)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57599031, rs386591895

HGVS names

This variant has 5 HGVS names - Hide

17:g.82209113G>T
ENST00000389641.8:c.-9+3672C>A
ENST00000582885.1:n.52-1065C>A
ENST00000392343.3:c.-326-1065C>A
ENST00000392347.5:c.-9+3672C>A

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 4 transcripts, has 3693 sample genotypes and is mentioned in 2 citations.

Variant displays