rs786201095

Orientation

minus

Stabilized

minus

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

Make rs786201095(G;G)

Make rs786201095(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

17028643

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs786201095
dbSNP (classic)	rs786201095
ClinGen	rs786201095
ebi	rs786201095
HLI	rs786201095
Exac	rs786201095
Gnomad	rs786201095
Varsome	rs786201095
LitVar	rs786201095
Map	rs786201095
PheGenI	rs786201095
Biobank	rs786201095
1000 genomes	rs786201095
hgdp	rs786201095
ensembl	rs786201095
geneview	rs786201095
scholar	rs786201095
google	rs786201095
pharmgkb	rs786201095
gwascentral	rs786201095
openSNP	rs786201095
23andMe	rs786201095
SNPshot	rs786201095
SNPdbe	rs786201095
MSV3d	rs786201095
GWAS Ctlg	rs786201095

Max Magnitude

0

ClinVar
Risk	rs786201095(G;G)
Alt	rs786201095(G;G)
Reference	Rs786201095(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Carney triad Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Variation	info
Gene	SDHB
CLNDBN	Hereditary cancer-predisposing syndrome Carney triad Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Reversed	1
HGVS	NC_000001.10:g.17355138A>C
CLNSRC	National Institutes of Health / The Eunice Kennedy Shriver National Institute of Child Health and Human Development
CLNACC	RCV000162628.3, RCV000170330.1, RCV000464351.1,