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 2:75633823 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.75633823C>T

Variation displays