Original source

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

A/G|Ancestral: A|Ambiguity code: R

Chromosome 11:112094831 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CD062227, CM012466

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 11374, 2010_April_001_296_SDHD_602690_0007

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and is associated with 3 phenotypes.

Variant displays