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
T/A | Ancestral: A | Ambiguity code: W
Location

Chromosome 17:1669184 (forward strand) | View in location tab

Co-located

with dbSNP rs368311418 (T/-)

Most severe consequence
Evidence status

This variation has 8 HGVS names - click the plus to show

Variation displays