Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 11:111958657 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021678

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11390, 2010_April_001_304_SDHD_602690_0023

This variation has 20 HGVS names - click the plus to show

Variation displays