This variation has been flagged

Flagged as suspect by dbSNP

Original source

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

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

Chromosome 6:161122046 (forward strand) | View in location tab

Most severe consequence
HGVS name

6:g.161122046C>T

Variation displays