Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.16 (T)
Location

Chromosome 11:126231037 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61401095, rs58255041

This variant has 10 HGVS names - click the plus to show

11:g.126231037C>T
ENST00000528985.5:c.-144+1744C>T
ENST00000533050.5:c.-8+1744C>T
ENST00000530043.5:c.-8+1701C>T
ENST00000525728.5:n.134+1744C>T
ENST00000627851.2:c.-8+1744C>T
ENST00000525338.1:c.-8+1744C>T
ENST00000360194.8:c.-7-3958C>T
ENST00000527247.5:n.70+1744C>T
ENST00000529731.5:c.-7-3958C>T

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 4543 sample genotypes.

Variant displays