rs786201063

Orientation

minus

Stabilized

minus

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

Make rs786201063(A;A)

Make rs786201063(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

17033059

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs786201063
dbSNP (classic)	rs786201063
ClinGen	rs786201063
ebi	rs786201063
HLI	rs786201063
Exac	rs786201063
Gnomad	rs786201063
Varsome	rs786201063
LitVar	rs786201063
Map	rs786201063
PheGenI	rs786201063
Biobank	rs786201063
1000 genomes	rs786201063
hgdp	rs786201063
ensembl	rs786201063
geneview	rs786201063
scholar	rs786201063
google	rs786201063
pharmgkb	rs786201063
gwascentral	rs786201063
openSNP	rs786201063
23andMe	rs786201063
SNPshot	rs786201063
SNPdbe	rs786201063
MSV3d	rs786201063
GWAS Ctlg	rs786201063

Max Magnitude

0

ClinVar
Risk	rs786201063(A;A)
Alt	rs786201063(A;A)
Reference	Rs786201063(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.17359554C>T
CLNSRC
CLNACC	RCV000162475.1,