Original source

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

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

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


with HGMD-PUBLIC CS083977

Most severe consequence
Intron variant
Evidence status

Clinical significance


LSDB SDHB_423+20T_A_061711

HGVS names

This variant has 8 HGVS names - 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