Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 11:69819192 (forward strand) | View in location tab

Most severe consequence
HGVS name

11:g.69819192G>C

Variation displays