rs778952116

Orientation

plus

Stabilized

plus

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

Make rs778952116(C;T)

Make rs778952116(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

17028736

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs778952116
dbSNP (classic)	rs778952116
ClinGen	rs778952116
ebi	rs778952116
HLI	rs778952116
Exac	rs778952116
Gnomad	rs778952116
Varsome	rs778952116
LitVar	rs778952116
Map	rs778952116
PheGenI	rs778952116
Biobank	rs778952116
1000 genomes	rs778952116
hgdp	rs778952116
ensembl	rs778952116
geneview	rs778952116
scholar	rs778952116
google	rs778952116
pharmgkb	rs778952116
gwascentral	rs778952116
openSNP	rs778952116
23andMe	rs778952116
SNPshot	rs778952116
SNPdbe	rs778952116
MSV3d	rs778952116
GWAS Ctlg	rs778952116

Max Magnitude

0

ClinVar
Risk	rs778952116(T;T)
Alt	rs778952116(T;T)
Reference	Rs778952116(C;C)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHB
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000001.10:g.17355231C>T
CLNSRC
CLNACC	RCV000492591.1,