rs121917755

Orientation

minus

Stabilized

minus

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

Make rs121917755(C;T)

Make rs121917755(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

17028724

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs121917755
dbSNP (classic)	rs121917755
ClinGen	rs121917755
ebi	rs121917755
HLI	rs121917755
Exac	rs121917755
Gnomad	rs121917755
Varsome	rs121917755
LitVar	rs121917755
Map	rs121917755
PheGenI	rs121917755
Biobank	rs121917755
1000 genomes	rs121917755
hgdp	rs121917755
ensembl	rs121917755
geneview	rs121917755
scholar	rs121917755
google	rs121917755
pharmgkb	rs121917755
gwascentral	rs121917755
openSNP	rs121917755
23andMe	rs121917755
SNPshot	rs121917755
SNPdbe	rs121917755
MSV3d	rs121917755
GWAS Ctlg	rs121917755

Max Magnitude

0

OMIM	185470
Desc
Variant	0011
Related	also

ClinVar
Risk	rs121917755(T;T)
Alt	rs121917755(T;T)
Reference	Rs121917755(C;C)
Significance	Pathogenic
Disease	Pheochromocytoma
Variation	info
Gene	SDHB
CLNDBN	Pheochromocytoma
Reversed	1
HGVS	NC_000001.10:g.17355219G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013629.26,