rs587782210

Orientation

plus

Stabilized

plus

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

Make rs587782210(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

112087959

Gene	SDHD, TIMM8B

is a	snp
is	mentioned by
dbSNP	rs587782210
dbSNP (classic)	rs587782210
ClinGen	rs587782210
ebi	rs587782210
HLI	rs587782210
Exac	rs587782210
Gnomad	rs587782210
Varsome	rs587782210
LitVar	rs587782210
Map	rs587782210
PheGenI	rs587782210
Biobank	rs587782210
1000 genomes	rs587782210
hgdp	rs587782210
ensembl	rs587782210
geneview	rs587782210
scholar	rs587782210
google	rs587782210
pharmgkb	rs587782210
gwascentral	rs587782210
openSNP	rs587782210
23andMe	rs587782210
SNPshot	rs587782210
SNPdbe	rs587782210
MSV3d	rs587782210
GWAS Ctlg	rs587782210

Max Magnitude

6.2

ClinVar
Risk	rs587782210(A;A)
Alt	rs587782210(A;A)
Reference	Rs587782210(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TIMM8B SDHD
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.111958683C>A
CLNSRC
CLNACC	RCV000130886.2,