Original source

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

HGVS names

This variant has 16 HGVS names - Hide

2:g.233759924C>T
ENST00000373445.1:c.856-7110C>T
ENST00000373409.7:c.868-7110C>T
ENST00000305139.10:c.862-7110C>T
ENST00000482026.5:c.868-7110C>T
ENST00000373424.5:c.61-7110C>T
ENST00000446481.6:c.61-7110C>T
ENST00000373426.3:c.856-7110C>T
ENST00000450233.1: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

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 22 transcripts, has 4171 sample genotypes, is associated with 8 phenotypes and is mentioned in 29 citations.

Variant displays