rs267607032

Orientation

minus

Stabilized

minus

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

Make rs267607032(G;T)

Make rs267607032(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

17028605

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs267607032
dbSNP (classic)	rs267607032
ClinGen	rs267607032
ebi	rs267607032
HLI	rs267607032
Exac	rs267607032
Gnomad	rs267607032
Varsome	rs267607032
LitVar	rs267607032
Map	rs267607032
PheGenI	rs267607032
Biobank	rs267607032
1000 genomes	rs267607032
hgdp	rs267607032
ensembl	rs267607032
geneview	rs267607032
scholar	rs267607032
google	rs267607032
pharmgkb	rs267607032
gwascentral	rs267607032
openSNP	rs267607032
23andMe	rs267607032
SNPshot	rs267607032
SNPdbe	rs267607032
MSV3d	rs267607032
GWAS Ctlg	rs267607032

Max Magnitude

0

ClinVar
Risk	rs267607032(T;T)
Alt	rs267607032(T;T)
Reference	Rs267607032(G;G)
Significance	Other
Disease	Paragangliomas 4 Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor Pheochromocytoma
Variation	info
Gene	SDHB
CLNDBN	Paragangliomas 4 Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor Pheochromocytoma
Reversed	1
HGVS	NC_000001.10:g.17355100C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013634.24, RCV000132167.4, RCV000234325.2,