Original source

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

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

Chromosome 5:147831830 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59354759, rs17625064

HGVS name

5:g.147831830A>G

This variation has assays on 10 chips - click the plus to show

Variation displays