Original source

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

C/G | Ancestral: C | Ambiguity code: S

Chromosome 12:48768470 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 269 sample genotypes.

Variant displays