Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.42 (T)
Location

Chromosome 17:65528964 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms
HGVS names

This variant has 6 HGVS names - Hide

17:g.65528964A>T
ENST00000618960.4:c.*1012T>A
ENST00000307078.9:c.*1012T>A
ENST00000611991.1:c.397-264T>A
LRG_296:g.37659T>A
LRG_296t1:c.*1012T>A

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 6 transcripts, has 4033 sample genotypes and is mentioned in 4 citations.

Variant displays