Original source

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

-/GGC | MAF: < 0.01 (GGC)

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