Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.25 (C)
Location

Chromosome 6:10420248 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58120572

HGVS name

6:g.10420248G>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 11 transcripts, has 1366 individual genotypes and is mentioned in 1 citation.

Variation displays