This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/A/C/T | Ancestral: G | Ambiguity code: N

Chromosome 1:17044882 (forward strand) | View in location tab


with HGMD-PUBLIC CD041934, CM020965

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB 5500, 2009_August_001_244_SDHB_185470_0006

This variant has 30 HGVS names - click the plus to show

About this variant

This variant overlaps 21 transcripts and is associated with 6 phenotypes.

Variant displays