Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.43 (C)
Location

Chromosome 19:17796030 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58123794, rs17750601

HGVS names

This variant has 5 HGVS names - Hide

19:g.17796030C>T
ENST00000600777.1:c.-51+857C>T
ENST00000599265.5:c.-51+1147C>T
ENST00000318683.6:c.-51+824C>T
ENST00000595387.1:c.-70+824C>T

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 4 transcripts, has 4307 sample genotypes and is mentioned in 2 citations.

Variant displays