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 10:101770052 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.101770052A>T

Variation displays