Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: < 0.01 (T)
Location

Chromosome 1:17028580 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS083977

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

LSDB SDHB_423+20T_A_061711

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 2504 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays