rs747198089

Orientation

plus

Stabilized

plus

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

Make rs747198089(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

17044873

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs747198089
dbSNP (classic)	rs747198089
ClinGen	rs747198089
ebi	rs747198089
HLI	rs747198089
Exac	rs747198089
Gnomad	rs747198089
Varsome	rs747198089
LitVar	rs747198089
Map	rs747198089
PheGenI	rs747198089
Biobank	rs747198089
1000 genomes	rs747198089
hgdp	rs747198089
ensembl	rs747198089
geneview	rs747198089
scholar	rs747198089
google	rs747198089
pharmgkb	rs747198089
gwascentral	rs747198089
openSNP	rs747198089
23andMe	rs747198089
SNPshot	rs747198089
SNPdbe	rs747198089
MSV3d	rs747198089
GWAS Ctlg	rs747198089

Max Magnitude

6.2

ClinVar
Risk	rs747198089(-;-)
Alt	rs747198089(-;-)
Reference	Rs747198089(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHB
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000001.10:g.17371368delG
CLNSRC
CLNACC	RCV000166126.2,