Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.36 (G)
Location

Chromosome 16:23622705 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 6 HGVS names - Hide

16:g.23622705A>G
ENST00000561764.1:n.420-1195A>G
ENST00000568219.5:c.2111+264T>C
ENST00000261584.8:c.2996+264T>C
LRG_308:g.23653T>C
LRG_308t1:c.2996+264T>C

Genotyping chips

This variant has assays on 14 chips - Show

About this variant

This variant overlaps 6 transcripts, has 4307 sample genotypes, is associated with 2 phenotypes and is mentioned in 19 citations.

Variant displays