rs786202732

Orientation

minus

Stabilized

minus

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

Make rs786202732(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

17024041

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs786202732
dbSNP (classic)	rs786202732
ClinGen	rs786202732
ebi	rs786202732
HLI	rs786202732
Exac	rs786202732
Gnomad	rs786202732
Varsome	rs786202732
LitVar	rs786202732
Map	rs786202732
PheGenI	rs786202732
Biobank	rs786202732
1000 genomes	rs786202732
hgdp	rs786202732
ensembl	rs786202732
geneview	rs786202732
scholar	rs786202732
google	rs786202732
pharmgkb	rs786202732
gwascentral	rs786202732
openSNP	rs786202732
23andMe	rs786202732
SNPshot	rs786202732
SNPdbe	rs786202732
MSV3d	rs786202732
GWAS Ctlg	rs786202732

Max Magnitude

6.2

ClinVar
Risk	rs786202732(C;C)
Alt	rs786202732(C;C)
Reference	Rs786202732(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	SDHB
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000001.10:g.17350536A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000165688.1, RCV000482399.1,