Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.28 (C)
Location

Chromosome 15:78453365 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57445303, rs386571355

This variant has 8 HGVS names - click the plus to show

15:g.78453365C>T
ENST00000560454.1:n.523-9557C>T
ENST00000258886.12:c.107-9557C>T
ENST00000560840.5:c.-65-9557C>T
ENST00000559215.5:c.107-11886C>T
ENST00000560440.5:c.107-9557C>T
ENST00000558525.5:c.102-9557C>T
ENST00000558570.5:c.107-9557C>T

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 3762 sample genotypes and is mentioned in 5 citations.

Variant displays