Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.41 (T)
Location

Chromosome 6:1614132 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58252855

HGVS name

6:g.1614132T>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays