Original source

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

Alleles
T/G | Ambiguity code: K
Location

Chromosome 8:6981012 (forward strand) | View in location tab

Co-located

with dbSNP rs62486787 (G/T)

Most severe consequence
HGVS name

8:g.6981012T>G

Variation displays