rs786201316

Orientation

minus

Stabilized

minus

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

Make rs786201316(GG;GG)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

17028712

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs786201316
dbSNP (classic)	rs786201316
ClinGen	rs786201316
ebi	rs786201316
HLI	rs786201316
Exac	rs786201316
Gnomad	rs786201316
Varsome	rs786201316
LitVar	rs786201316
Map	rs786201316
PheGenI	rs786201316
Biobank	rs786201316
1000 genomes	rs786201316
hgdp	rs786201316
ensembl	rs786201316
geneview	rs786201316
scholar	rs786201316
google	rs786201316
pharmgkb	rs786201316
gwascentral	rs786201316
openSNP	rs786201316
23andMe	rs786201316
SNPshot	rs786201316
SNPdbe	rs786201316
MSV3d	rs786201316
GWAS Ctlg	rs786201316

Max Magnitude

6.2

ClinVar
Risk	rs786201316(GG;GG)
Alt	rs786201316(GG;GG)
Reference	Rs786201316(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHB
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000001.10:g.17355207delTinsCC
CLNSRC
CLNACC	RCV000163361.2,