Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

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

10:g.81883883C>G
ENST00000602794.4:c.61-5307C>G
ENST00000555784.4:c.135+5788C>G
ENST00000404547.4:c.823+7720C>G
ENST00000404576.5:c.135+5788C>G
ENST00000372142.5:c.60+5863C>G
ENST00000556918.4:c.135+5788C>G
ENST00000372141.5:c.823+7720C>G

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 7 transcripts, has 2833 individual genotypes and is mentioned in 3 citations.

Variation displays