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 4:154562561 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.154562561C>T

Variation displays