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 | MAF: 0.03 (C)
Location

Chromosome 11:6388699 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.6388699G>C

Variation displays