Original source

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

Alleles
T/C/G|Ancestral: T|Ambiguity code: B
Location

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

Co-located variant

HGMD-PUBLIC CM040488

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_247_SDHB_185470_0010, 5504

HGVS names

This variant has 24 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and is associated with 2 phenotypes.

Variant displays