rs878854594

Orientation

plus

Stabilized

plus

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

Make rs878854594(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

112094851

Gene

SDHD

is a	snp
is	mentioned by
dbSNP	rs878854594
dbSNP (classic)	rs878854594
ClinGen	rs878854594
ebi	rs878854594
HLI	rs878854594
Exac	rs878854594
Gnomad	rs878854594
Varsome	rs878854594
LitVar	rs878854594
Map	rs878854594
PheGenI	rs878854594
Biobank	rs878854594
1000 genomes	rs878854594
hgdp	rs878854594
ensembl	rs878854594
geneview	rs878854594
scholar	rs878854594
google	rs878854594
pharmgkb	rs878854594
gwascentral	rs878854594
openSNP	rs878854594
23andMe	rs878854594
SNPshot	rs878854594
SNPdbe	rs878854594
MSV3d	rs878854594
GWAS Ctlg	rs878854594

Max Magnitude

6.2

ClinVar
Risk	rs878854594(T;T)
Alt	rs878854594(T;T)
Reference	Rs878854594(C;C)
Significance	Probable-Pathogenic
Disease	Paraganglioma and gastric stromal sarcoma Paragangliomas 1 Pheochromocytoma
Variation	info
Gene	SDHD
CLNDBN	Paraganglioma and gastric stromal sarcoma Paragangliomas 1 Pheochromocytoma
Reversed	0
HGVS	NC_000011.9:g.111965575C>T
CLNSRC
CLNACC	RCV000226232.1,