Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 10:82273509 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

10:g.82273509A>G
ENST00000602794.3:c.*372-85230A>G
ENST00000555784.3:c.136-85230A>G
ENST00000404547.3:c.824-85230A>G
ENST00000404576.4:c.236-85230A>G
ENST00000556918.3:c.313+40690A>G
ENST00000372142.4:c.161-85230A>G
ENST00000372141.4:c.824-85230A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays