Original source

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

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

Chromosome 5:161846288 (forward strand) | View in location tab

Most severe consequence
HGVS name

5:g.161846288A>T

Variation displays