Original source

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

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

Chromosome 7:39016221 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.39016221T>C

Variation displays