rs587781270

Orientation

minus

Stabilized

minus

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

Make rs587781270(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

17033058

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs587781270
dbSNP (classic)	rs587781270
ClinGen	rs587781270
ebi	rs587781270
HLI	rs587781270
Exac	rs587781270
Gnomad	rs587781270
Varsome	rs587781270
LitVar	rs587781270
Map	rs587781270
PheGenI	rs587781270
Biobank	rs587781270
1000 genomes	rs587781270
hgdp	rs587781270
ensembl	rs587781270
geneview	rs587781270
scholar	rs587781270
google	rs587781270
pharmgkb	rs587781270
gwascentral	rs587781270
openSNP	rs587781270
23andMe	rs587781270
SNPshot	rs587781270
SNPdbe	rs587781270
MSV3d	rs587781270
GWAS Ctlg	rs587781270

Max Magnitude

6.2

ClinVar
Risk	rs587781270(A;A)
Alt	rs587781270(A;A)
Reference	Rs587781270(T;T)
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.17359553A>T
CLNSRC
CLNACC	RCV000128905.4, RCV000475161.1, RCV000481752.1,