rs587782604

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs587782604(A;A)

Make rs587782604(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

17022684

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs587782604
dbSNP (classic)	rs587782604
ClinGen	rs587782604
ebi	rs587782604
HLI	rs587782604
Exac	rs587782604
Gnomad	rs587782604
Varsome	rs587782604
LitVar	rs587782604
Map	rs587782604
PheGenI	rs587782604
Biobank	rs587782604
1000 genomes	rs587782604
hgdp	rs587782604
ensembl	rs587782604
geneview	rs587782604
scholar	rs587782604
google	rs587782604
pharmgkb	rs587782604
gwascentral	rs587782604
openSNP	rs587782604
23andMe	rs587782604
SNPshot	rs587782604
SNPdbe	rs587782604
MSV3d	rs587782604
GWAS Ctlg	rs587782604

Max Magnitude

0

ClinVar
Risk	rs587782604(A;A) rs587782604(T;T)
Alt	rs587782604(A;A) rs587782604(T;T)
Reference	Rs587782604(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.17349179C>A; NC_000001.10:g.17349179C>T
CLNSRC
CLNACC	RCV000164275.2, RCV000473831.1, RCV000131970.4, RCV000183215.3, RCV000456660.1,