Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.01 (A)
Location

Chromosome 5:161846043 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

5:g.161846043C>A

Variation displays