rs74315371

Orientation

minus

Stabilized

minus

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

Make rs74315371(A;A)

Reference

GRCh38 38.1/141

Chromosome

1

Position

17028721

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs74315371
dbSNP (classic)	rs74315371
ClinGen	rs74315371
ebi	rs74315371
HLI	rs74315371
Exac	rs74315371
Gnomad	rs74315371
Varsome	rs74315371
LitVar	rs74315371
Map	rs74315371
PheGenI	rs74315371
Biobank	rs74315371
1000 genomes	rs74315371
hgdp	rs74315371
ensembl	rs74315371
geneview	rs74315371
scholar	rs74315371
google	rs74315371
pharmgkb	rs74315371
gwascentral	rs74315371
openSNP	rs74315371
23andMe	rs74315371
SNPshot	rs74315371
SNPdbe	rs74315371
MSV3d	rs74315371
GWAS Ctlg	rs74315371

Max Magnitude

6.2

OMIM	185470
Desc
Variant	0009
Related	also

ClinVar
Risk	rs74315371(A;A)
Alt	rs74315371(A;A)
Reference	Rs74315371(G;G)
Significance	Pathogenic
Disease	Pheochromocytoma
Variation	info
Gene	SDHB
CLNDBN	Pheochromocytoma
Reversed	1
HGVS	NC_000001.10:g.17355216C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013627.25,