Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 11:112088939 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM000207, CD094779

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11370, NM_003002.1:c.242C>T, 2010_April_001_293_SDHD_602690_0003

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

Variation displays