Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 1:17028721 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM020967

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5503, 2009_August_001_246_SDHB_185470_0009

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and is associated with 2 phenotypes.

Variant displays