Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: < 0.01 (A)
Location

Chromosome 6:33386189 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.33386189C>A

Variation displays