Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.30 (T)
Location

Chromosome 20:2380344 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3854714, rs58766410

HGVS name

20:g.2380344T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays