rs786201161

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs786201161(A;G)

Make rs786201161(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

17024076

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs786201161
dbSNP (classic)	rs786201161
ClinGen	rs786201161
ebi	rs786201161
HLI	rs786201161
Exac	rs786201161
Gnomad	rs786201161
Varsome	rs786201161
LitVar	rs786201161
Map	rs786201161
PheGenI	rs786201161
Biobank	rs786201161
1000 genomes	rs786201161
hgdp	rs786201161
ensembl	rs786201161
geneview	rs786201161
scholar	rs786201161
google	rs786201161
pharmgkb	rs786201161
gwascentral	rs786201161
openSNP	rs786201161
23andMe	rs786201161
SNPshot	rs786201161
SNPdbe	rs786201161
MSV3d	rs786201161
GWAS Ctlg	rs786201161

Max Magnitude

0

ClinVar
Risk	rs786201161(G;G)
Alt	rs786201161(G;G)
Reference	Rs786201161(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome SDHB-Related Disorders
Variation	info
Gene	SDHB
CLNDBN	Hereditary cancer-predisposing syndrome SDHB-Related Disorders
Reversed	1
HGVS	NC_000001.10:g.17350571T>C
CLNSRC
CLNACC	RCV000162804.2, RCV000374774.1,