Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 11:112088971 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM000208

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_003002.1:c.274G>T, 2010_April_001_294_SDHD_602690_0004, 11371

This variation has 23 HGVS names - click the plus to show

About this variant

This variant overlaps 20 transcripts, is associated with 4 phenotypes and is mentioned in 3 citations.

Variation displays