Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs13301155, rs386547861

HGVS names

This variant has 4 HGVS names - Hide

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

Genotyping chips

This variant has assays on 8 chips - 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 31 citations.

Variant displays