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 7:101125693 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.101125693C>T

Variation displays