Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.45 (C)
Location

Chromosome 11:72245855 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.72245855C>G

Variation displays