Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 8:48922748 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

8:g.48922748G>C

About this variant

This variant overlaps 2 transcripts and 1 regulatory feature.

Variant displays