Original source

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

Alleles
-/C | MAF: < 0.01 (-)
Location

Chromosome 19: between 7958504 and 7958505 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.7958504dupC

Variation displays