rs587782243

Orientation

minus

Stabilized

minus

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

Make rs587782243(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

17033060

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs587782243
dbSNP (classic)	rs587782243
ClinGen	rs587782243
ebi	rs587782243
HLI	rs587782243
Exac	rs587782243
Gnomad	rs587782243
Varsome	rs587782243
LitVar	rs587782243
Map	rs587782243
PheGenI	rs587782243
Biobank	rs587782243
1000 genomes	rs587782243
hgdp	rs587782243
ensembl	rs587782243
geneview	rs587782243
scholar	rs587782243
google	rs587782243
pharmgkb	rs587782243
gwascentral	rs587782243
openSNP	rs587782243
23andMe	rs587782243
SNPshot	rs587782243
SNPdbe	rs587782243
MSV3d	rs587782243
GWAS Ctlg	rs587782243

Max Magnitude

6.2

ClinVar
Risk	rs587782243(A;A)
Alt	rs587782243(A;A)
Reference	Rs587782243(G;G)
Significance	Probable-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.17359555C>T
CLNSRC
CLNACC	RCV000130946.4, RCV000459169.1, RCV000489952.1,