Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: < 0.01 (T)
Location

Chromosome 9:124450082 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

9:g.124450082A>T

Variation displays