Original source

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

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

Chromosome 15:43203237 (forward strand) | View in location tab

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB NG_011505.1:g.22889G>T_1341605555

HGVS names

This variant has 24 HGVS names - Show

About this variant

This variant overlaps 16 transcripts, has 2504 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays