Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.27 (A)
Location

Chromosome 9:114804160 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 2 HGVS names - Hide

9:g.114804160A>G
ENST00000374045.4:c.210+1643T>C

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 6004 sample genotypes, is associated with 2 phenotypes and is mentioned in 26 citations.

Variant displays