Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.10 (T)
Location

Chromosome 11:117661016 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57276883, rs56525925

HGVS names

This variant has 3 HGVS names - Hide

11:g.117661016C>T
ENST00000527706.5:c.102+119739G>A
ENST00000321322.6:c.691+115775G>A

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3967 sample genotypes, is associated with 1 phenotype and is mentioned in 5 citations.

Variant displays