rs397516833

Orientation

minus

Stabilized

minus

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

Make rs397516833(C;C)

Make rs397516833(C;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

17028737

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs397516833
dbSNP (classic)	rs397516833
ClinGen	rs397516833
ebi	rs397516833
HLI	rs397516833
Exac	rs397516833
Gnomad	rs397516833
Varsome	rs397516833
LitVar	rs397516833
Map	rs397516833
PheGenI	rs397516833
Biobank	rs397516833
1000 genomes	rs397516833
hgdp	rs397516833
ensembl	rs397516833
geneview	rs397516833
scholar	rs397516833
google	rs397516833
pharmgkb	rs397516833
gwascentral	rs397516833
openSNP	rs397516833
23andMe	rs397516833
SNPshot	rs397516833
SNPdbe	rs397516833
MSV3d	rs397516833
GWAS Ctlg	rs397516833

Max Magnitude

0

ClinVar
Risk	rs397516833(C;C)
Alt	rs397516833(C;C)
Reference	Rs397516833(G;G)
Significance	Pathogenic
Disease	Hereditary Paraganglioma-Pheochromocytoma Syndromes Hereditary cancer-predisposing syndrome Paragangliomas 4 Pheochromocytoma not provided
Variation	info
Gene	SDHB
CLNDBN	Hereditary Paraganglioma-Pheochromocytoma Syndromes Hereditary cancer-predisposing syndrome Paragangliomas 4 Pheochromocytoma not provided
Reversed	1
HGVS	NC_000001.10:g.17355232C>G
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000037719.2, RCV000128907.3, RCV000332692.1, RCV000387244.1, RCV000478921.1,