rs876658367

Orientation

minus

Stabilized

minus

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

Make rs876658367(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

17024028

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs876658367
dbSNP (classic)	rs876658367
ClinGen	rs876658367
ebi	rs876658367
HLI	rs876658367
Exac	rs876658367
Gnomad	rs876658367
Varsome	rs876658367
LitVar	rs876658367
Map	rs876658367
PheGenI	rs876658367
Biobank	rs876658367
1000 genomes	rs876658367
hgdp	rs876658367
ensembl	rs876658367
geneview	rs876658367
scholar	rs876658367
google	rs876658367
pharmgkb	rs876658367
gwascentral	rs876658367
openSNP	rs876658367
23andMe	rs876658367
SNPshot	rs876658367
SNPdbe	rs876658367
MSV3d	rs876658367
GWAS Ctlg	rs876658367

Max Magnitude

6.2

ClinVar
Risk	rs876658367(A;A)
Alt	rs876658367(A;A)
Reference	Rs876658367(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma not provided
Variation	info
Gene	SDHB
CLNDBN	Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma not provided
Reversed	1
HGVS	NC_000001.10:g.17350523C>T
CLNSRC
CLNACC	RCV000220162.1, RCV000461924.1, RCV000479413.1,