Original source

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

Alleles
G/A | Ambiguity code: R
Location

Chromosome Y:9543684 (forward strand) | View in location tab

Most severe consequence
HGVS name

Y:g.9543684G>A

Variation displays