Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 20:58650412 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.58650412C>T

Genotyping chips

This variation has assays on: Illumina_1M-duo

Variation displays