Original source

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

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

Chromosome 6:98832998 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

6:g.98832998C>G

About this variant

This variant overlaps 1 transcript.

Variant displays