Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.28 (C)
Location

Chromosome 9:114796423 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61572525

HGVS names

This variant has 2 HGVS names - Hide

9:g.114796423C>T
ENST00000374045.4:c.211-2855G>A

Genotyping chips

This variant has assays on 14 chips - Show

About this variant

This variant overlaps 2 transcripts, has 6275 sample genotypes, is associated with 3 phenotypes and is mentioned in 27 citations.

Variant displays