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 2:75860949 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.75860949C>T

Variation displays