Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A | Ambiguity code: R
Location

Chromosome 12:106356588 (forward strand) | View in location tab

Co-located

with dbSNP rs375627927 (G/-)

Most severe consequence
Evidence status

HGVS name

12:g.106356588G>A

Variation displays