Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.40 (C)
Location

Chromosome 11:132012913 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59281186

HGVS names

This variant has 8 HGVS names - Hide

11:g.132012913C>T
ENST00000374784.5:c.167+101265C>T
ENST00000479431.1:n.208+101265C>T
ENST00000374791.7:c.167+101265C>T
ENST00000498764.5:n.143+101265C>T
ENST00000374786.5:c.167+101265C>T
ENST00000550167.5:c.140+101265C>T
ENST00000425719.6:c.167+101265C>T

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 7 transcripts and has 6072 sample genotypes.

Variant displays