Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 4:3461931 (forward strand) | View in location tab

Most severe consequence
HGVS name

4:g.3461931T>A

Variation displays