Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.05 (C)
Location

Chromosome 10:82192849 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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

10:g.82192849T>C
ENST00000602794.5:c.*372-165890T>C
ENST00000555784.5:c.136-165890T>C
ENST00000404547.5:c.824-165890T>C
ENST00000404576.6:c.235+26023T>C
ENST00000372142.6:c.160+26023T>C
ENST00000556918.5:c.235+26023T>C
ENST00000372141.6:c.824-165890T>C

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 2669 sample genotypes and is mentioned in 1 citation.

Variant displays