Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.14 (G)
Location

Chromosome 10:81883883 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 8 HGVS names - Hide

10:g.81883883C>G
ENST00000602794.5:c.61-5307C>G
ENST00000555784.5:c.135+5788C>G
ENST00000404547.5:c.823+7720C>G
ENST00000404576.6:c.135+5788C>G
ENST00000372142.6:c.60+5863C>G
ENST00000556918.5:c.135+5788C>G
ENST00000372141.6:c.823+7720C>G

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 7 transcripts, has 3779 sample genotypes and is mentioned in 3 citations.

Variant displays