Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 1:17033078 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012800

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_241_SDHB_185470_0001, 5495, SDHB_268C_T_061511

This variation has 13 HGVS names - click the plus to show

Variation displays