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

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

Chromosome 1:17028628 (forward strand) | View in location tab


with HGMD-PUBLIC CM040488

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 5504, 2009_August_001_247_SDHB_185470_0010

This variant has 36 HGVS names - click the plus to show

About this variant

This variant overlaps 21 transcripts and is associated with 2 phenotypes.

Variant displays