Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 12:21852380 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB ABCC9_2631G_A_082010

This variation has 8 HGVS names - click the plus to show

About this variant

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

Variation displays