rs876658461

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6.2	Hereditary PGL/PCC Syndrome

Make rs876658461(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

17023975

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs876658461
dbSNP (classic)	rs876658461
ClinGen	rs876658461
ebi	rs876658461
HLI	rs876658461
Exac	rs876658461
Gnomad	rs876658461
Varsome	rs876658461
LitVar	rs876658461
Map	rs876658461
PheGenI	rs876658461
Biobank	rs876658461
1000 genomes	rs876658461
hgdp	rs876658461
ensembl	rs876658461
geneview	rs876658461
scholar	rs876658461
google	rs876658461
pharmgkb	rs876658461
gwascentral	rs876658461
openSNP	rs876658461
23andMe	rs876658461
SNPshot	rs876658461
SNPdbe	rs876658461
MSV3d	rs876658461
GWAS Ctlg	rs876658461

Max Magnitude

6.2

ClinVar
Risk	rs876658461(T;T)
Alt	rs876658461(T;T)
Reference	Rs876658461(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Paragangliomas 4 Gastrointestinal stromal tumor Pheochromocytoma
Variation	info
Gene	SDHB
CLNDBN	Hereditary cancer-predisposing syndrome Paragangliomas 4 Gastrointestinal stromal tumor Pheochromocytoma
Reversed	1
HGVS	NC_000001.10:g.17350470G>A
CLNSRC
CLNACC	RCV000215175.1, RCV000238597.1, RCV000472972.1,