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: 0.19 (G)
Location

Chromosome 5:126595330 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58596945

This variation has 5 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays