Original source

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

Alleles
-/GGC|MAF: < 0.01 (GGC)
Location

Chromosome 12: between 48766731 and 48766732 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2504 sample genotypes.

Variant displays