Original source

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

Alleles
G/A | Ambiguity code: R
Location

Chromosome 12:106750366 (forward strand) | View in location tab

Co-located

with dbSNP rs375627927 (G/-)

Most severe consequence
Evidence status

HGVS name

12:g.106750366G>A

Variation displays