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 5:132294030 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and 1 regulatory feature.

Variant displays