Original source

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

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

Chromosome 1:17022648 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020970

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5498, 2009_August_001_243_SDHB_185470_0004

This variation has 9 HGVS names - click the plus to show

Variation displays