Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
 
Upstream gene variant
HGVS name

12:g.106356588G>A

About this variant

This variant overlaps 2 transcripts and has 1 sample genotype.

Variant displays