Original source

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

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

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


with HGMD-PUBLIC CM012800

Most severe consequence
Evidence status

Clinical significance


LSDB 2009_August_001_241_SDHB_185470_0001, 5495, SDHB_268C_T_061511

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

About this variant

This variant overlaps 7 transcripts, has 1092 individual genotypes, is associated with 4 phenotypes and is mentioned in 5 citations.

Variation displays