Original source

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

Alleles
T/G | Ambiguity code: K | MAF: < 0.01 (G)
Location

Chromosome 11:18285887 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.18285887T>G

Variation displays