Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.27 (A)
Location

Chromosome 1:48509774 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

1:g.48509774A>G

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Affy GenomeWideSNP_6.0

Variation displays