Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | 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
Evidence status

Clinical significance

Synonyms

LSDB SDHB_423+20T_A_061711

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

Variation displays