Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.03 (A)
Location

Chromosome 4:155504223 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.155504223G>A

Variation displays