Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.15 (A)
Location

Chromosome 4:155504038 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.155504038G>A

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

Variation displays