Original source

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

Alleles
G/C | Ambiguity code: S | MAF: 0.37 (C)
Location

Chromosome 1:8923596 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59480103

HGVS name

1:g.8923596G>C

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

Variation displays