Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.16 (G)
Location

Chromosome 1:153258885 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.153258885C>G

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Illumina_HumanOmni5, Illumina_1M-duo

Variation displays