Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R
Location

Chromosome 4:74606108 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.74606108G>A

Variation displays