Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 20:759656 (forward strand) | View in location tab

Most severe consequence
HGVS name

20:g.759656C>T

Variation displays