Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.01 (C)
Location

Chromosome 6:34395673 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

6:g.34395673C>T

Variation displays