Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome 7:27241277 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

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

About this variant

This variant overlaps 14 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays