Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.35 (C)
Location

Chromosome 19:50025640 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

This variant has 3 HGVS names - click the plus to show

19:g.50025640C>T
ENST00000599538.5:c.-359G>A
ENST00000596445.5:c.-65+28G>A

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

About this variant

This variant overlaps 28 transcripts, 1 regulatory feature, has 3755 sample genotypes and is mentioned in 1 citation.

Variant displays