Original source

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

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

Chromosome 7:38976623 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.38976623T>C

Variation displays