Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.04 (G)
Location

Chromosome 10:84033265 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

10:g.84033265A>G
ENST00000602794.1:c.*372-85230A>G
ENST00000555784.1:c.136-85230A>G
ENST00000404547.1:c.824-85230A>G
ENST00000404576.2:c.236-85230A>G
ENST00000372142.2:c.161-85230A>G
ENST00000556918.1:c.313+40690A>G
ENST00000372141.2:c.824-85230A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays