Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 11:112086910 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM013281, CM092619

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11382, 2010_April_001_300_SDHD_602690_0015, NM_003002.1:c.3G>C

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

Variation displays