Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 6 HGVS names - click the plus to show

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

This variant has assays on 4 chips - click the plus to show

About this variant

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

Variant displays