Original source

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

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

Chromosome 11:34458915 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.34458915G>C

Variation displays