Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Clinical significance

Synonyms

LSDB ABCC9_-11T_C_090610

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 2504 individual genotypes and is associated with 1 phenotype.

Variation displays