rs786203800

Orientation

minus

Stabilized

minus

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

Make rs786203800(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

17053994

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs786203800
dbSNP (classic)	rs786203800
ClinGen	rs786203800
ebi	rs786203800
HLI	rs786203800
Exac	rs786203800
Gnomad	rs786203800
Varsome	rs786203800
LitVar	rs786203800
Map	rs786203800
PheGenI	rs786203800
Biobank	rs786203800
1000 genomes	rs786203800
hgdp	rs786203800
ensembl	rs786203800
geneview	rs786203800
scholar	rs786203800
google	rs786203800
pharmgkb	rs786203800
gwascentral	rs786203800
openSNP	rs786203800
23andMe	rs786203800
SNPshot	rs786203800
SNPdbe	rs786203800
MSV3d	rs786203800
GWAS Ctlg	rs786203800

Max Magnitude

6.2

ClinVar
Risk	rs786203800(A;A)
Alt	rs786203800(A;A)
Reference	Rs786203800(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHB
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000001.10:g.17380489A>T
CLNSRC
CLNACC	RCV000167262.2,