Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.31 (T)
Location

Chromosome 9:104902020 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386547861, rs13301155

This variant has 4 HGVS names - click the plus to show

9:g.104902020C>T
ENST00000374733.1:c.-114-12825G>A
ENST00000374736.7:c.66+1594G>A
ENST00000423487.6:c.66+1594G>A

This variant has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 3962 sample genotypes, is associated with 8 phenotypes and is mentioned in 28 citations.

Variant displays