rs587776644

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;T)	6.2	Hereditary PGL/PCC Syndrome
(T;T)	0	common in clinvar

Make rs587776644(G;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

112086961

Gene	SDHD, TIMM8B

is a	snp
is	mentioned by
dbSNP	rs587776644
dbSNP (classic)	rs587776644
ClinGen	rs587776644
ebi	rs587776644
HLI	rs587776644
Exac	rs587776644
Gnomad	rs587776644
Varsome	rs587776644
LitVar	rs587776644
Map	rs587776644
PheGenI	rs587776644
Biobank	rs587776644
1000 genomes	rs587776644
hgdp	rs587776644
ensembl	rs587776644
geneview	rs587776644
scholar	rs587776644
google	rs587776644
pharmgkb	rs587776644
gwascentral	rs587776644
openSNP	rs587776644
23andMe	rs587776644
SNPshot	rs587776644
SNPdbe	rs587776644
MSV3d	rs587776644
GWAS Ctlg	rs587776644

Max Magnitude

6.2

ClinVar
Risk	rs587776644(G;G)
Alt	rs587776644(G;G)
Reference	Rs587776644(T;T)
Significance	Pathogenic
Disease	Paragangliomas 1
Variation	info
Gene	TIMM8B SDHD
CLNDBN	Paragangliomas 1
Reversed	0
HGVS	NC_000011.9:g.111957685T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007298.2,