Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.35 (T)
Location

Chromosome 2:233759924 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 17 HGVS names - click the plus to show

2:g.233759924C>T
ENST00000373445.1:c.856-7110C>T
ENST00000305139.10:c.862-7110C>T
ENST00000373409.7:c.868-7110C>T
ENST00000482026.5:c.868-7110C>T
ENST00000446481.6:c.61-7110C>T
ENST00000373424.5:c.61-7110C>T
ENST00000373426.3:c.856-7110C>T
ENST00000450233.1:c.868-7110C>T
ENST00000609767.2:c.868-7110C>T
ENST00000373414.3:c.868-7110C>T
ENST00000406651.1:c.61-7110C>T
ENST00000373450.4:c.856-7110C>T
ENST00000344644.9:c.856-7110C>T
ENST00000354728.4:c.856-7110C>T
ENST00000484784.2:c.*238-7110C>T
LRG_733:g.4652C>T

This variant has assays on 13 chips - click the plus to show

About this variant

This variant overlaps 23 transcripts, has 4171 sample genotypes, is associated with 8 phenotypes and is mentioned in 25 citations.

Variant displays