Original source

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

Alleles
C/G | Ancestral: T | Ambiguity code: S | MAF: < 0.01 (G)
Location

Chromosome 11:2016397 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.2016397C>G

Variation displays