Original source

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

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

Chromosome 13:48806688 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

13:g.48806688G>T

Variation displays