Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.24 (A)
Location

Chromosome 13:48232374 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

13:g.48232374G>A

This variation has assays on 7 chips - click the plus to show

Variation displays