Original source

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

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

Chromosome 12:21818153 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB ABCC9_3768T_C_091310

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays