Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.26 (A)
Location

Chromosome 16:68787043 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59368541

HGVS names

This variant has 13 HGVS names - Hide

16:g.68787043G>A
ENST00000611625.4:c.164-14627G>A
ENST00000564676.5:n.446-14627G>A
ENST00000612417.4:c.164-14627G>A
ENST00000566612.5:c.164-14627G>A
ENST00000621016.4:c.164-14627G>A
ENST00000422392.6:c.164-14627G>A
ENST00000564745.1:n.159-14627G>A
ENST00000261769.9:c.164-14627G>A
ENST00000566510.5:c.164-14627G>A
ENST00000562836.5:n.235-14627G>A
LRG_301:g.54752G>A
LRG_301t1:c.164-14627G>A

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 11 transcripts, 1 regulatory feature, has 3693 sample genotypes, is associated with 1 phenotype and is mentioned in 53 citations.

Variant displays