Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.23 (T)
Location

Chromosome 7:16087084 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17169257

HGVS name

7:g.16087084A>T

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

Variation displays