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 15:64164156 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts.

Variant displays