Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

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


with HGMD-PUBLIC CM092619, CM013281

Most severe consequence
Start lost
Evidence status

Clinical significance


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

HGVS names

This variant has 20 HGVS names - Show

About this variant

This variant overlaps 24 transcripts, 1 regulatory feature, is associated with 3 phenotypes and is mentioned in 2 citations.

Variant displays