Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.22 (T)
Location

Chromosome 16:79066662 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 6 HGVS names - Hide

16:g.79066662A>T
ENST00000406884.6:c.517-144946A>T
ENST00000539474.6:c.486-144946A>T
ENST00000402655.6:c.410-144946A>T
ENST00000569332.5:c.*854-144946A>T
ENST00000566780.5:c.1057-144946A>T

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 5 transcripts, has 4303 sample genotypes and is mentioned in 1 citation.

Variant displays