Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.38 (A)
Location

Chromosome 10:49607466 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17719152, rs58882174

HGVS name

10:g.49607466G>A

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

Variation displays