rs786201085

Orientation

minus

Stabilized

minus

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

Make rs786201085(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

17022615

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs786201085
dbSNP (classic)	rs786201085
ClinGen	rs786201085
ebi	rs786201085
HLI	rs786201085
Exac	rs786201085
Gnomad	rs786201085
Varsome	rs786201085
LitVar	rs786201085
Map	rs786201085
PheGenI	rs786201085
Biobank	rs786201085
1000 genomes	rs786201085
hgdp	rs786201085
ensembl	rs786201085
geneview	rs786201085
scholar	rs786201085
google	rs786201085
pharmgkb	rs786201085
gwascentral	rs786201085
openSNP	rs786201085
23andMe	rs786201085
SNPshot	rs786201085
SNPdbe	rs786201085
MSV3d	rs786201085
GWAS Ctlg	rs786201085

Max Magnitude

6.2

ClinVar
Risk	rs786201085(A;A)
Alt	rs786201085(A;A)
Reference	Rs786201085(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.17349110C>T
CLNSRC
CLNACC	RCV000162580.2,