Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.34 (G)
Location

Chromosome 9:99153883 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57580963

This variation has 2 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

Variation displays