rs876659330

Orientation

minus

Stabilized

minus

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

Make rs876659330(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

17044758

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs876659330
dbSNP (classic)	rs876659330
ClinGen	rs876659330
ebi	rs876659330
HLI	rs876659330
Exac	rs876659330
Gnomad	rs876659330
Varsome	rs876659330
LitVar	rs876659330
Map	rs876659330
PheGenI	rs876659330
Biobank	rs876659330
1000 genomes	rs876659330
hgdp	rs876659330
ensembl	rs876659330
geneview	rs876659330
scholar	rs876659330
google	rs876659330
pharmgkb	rs876659330
gwascentral	rs876659330
openSNP	rs876659330
23andMe	rs876659330
SNPshot	rs876659330
SNPdbe	rs876659330
MSV3d	rs876659330
GWAS Ctlg	rs876659330

Max Magnitude

6.2

ClinVar
Risk	rs876659330(C;C)
Alt	rs876659330(C;C)
Reference	Rs876659330(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHB
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000001.10:g.17371253C>G
CLNSRC
CLNACC	RCV000221442.2,