Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V
Location

Chromosome 1:17044882 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020965, CD041934

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5500, 2009_August_001_244_SDHB_185470_0006

This variation has 22 HGVS names - click the plus to show

Variation displays