Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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

Co-located

with HGMD-PUBLIC CM040488

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5504, 2009_August_001_247_SDHB_185470_0010

This variation has 24 HGVS names - click the plus to show

Variation displays