Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/C|Ambiguity code: S
Location

Chromosome 12:52316292 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript, 1 regulatory feature and has 2 sample genotypes.

Variant displays