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 | MAF: < 0.01 (T)
Location

Chromosome 14:102080677 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

14:g.102080677C>T

Variation displays