Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: < 0.01 (G)
Location

Chromosome 12:21936685 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Clinical significance

Synonyms

LSDB ABCC9_-11T_C_090610

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays