Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W|MAF: 0.49 (A)
Location

Chromosome 16:58521649 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59662370, rs59076330

HGVS names

This variant has 7 HGVS names - Hide

16:g.58521649T>A
ENST00000317147.9:c.6918-332A>T
ENST00000569924.1:n.337-332A>T
ENST00000569240.5:c.6903-332A>T
ENST00000245138.8:c.932-332A>T
ENST00000567188.5:c.*633-332A>T
ENST00000563130.5:n.1793-332A>T

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 17 transcripts, 1 regulatory feature, has 4042 sample genotypes and is mentioned in 1 citation.

Variant displays