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
A/G | Ambiguity code: R
Location

Chromosome 7:76067200 (forward strand) | View in location tab

Co-located

with dbSNP rs112106018 (C/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1799219

This variation has 7 HGVS names - click the plus to show

Variation displays