Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.13 (G)
Location

Chromosome 5:147211393 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59354759, rs17625064

HGVS name

5:g.147211393A>G

This variation has assays on 9 chips - click the plus to show

Variation displays