Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.44 (A)
Location

Chromosome 5:147204592 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17625017, rs59148813

This variation has 3 HGVS names - click the plus to show

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

Variation displays