Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.08 (A)
Location

Chromosome 7:97020059 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

7:g.97020059G>A

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

Variation displays