Original source

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

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

Chromosome 11:111959695 (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 22 HGVS names - click the plus to show

Variation displays