Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
HGVS names

This variant has 8 HGVS names - Hide

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
ENST00000556918.5:c.235+26023T>C
ENST00000372142.6:c.160+26023T>C
ENST00000372141.6:c.824-165890T>C

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 7 transcripts, has 3093 sample genotypes and is mentioned in 1 citation.

Variant displays