rs876659276

Orientation

plus

Stabilized

plus

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

Make rs876659276(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

112094830

Gene

SDHD

is a	snp
is	mentioned by
dbSNP	rs876659276
dbSNP (classic)	rs876659276
ClinGen	rs876659276
ebi	rs876659276
HLI	rs876659276
Exac	rs876659276
Gnomad	rs876659276
Varsome	rs876659276
LitVar	rs876659276
Map	rs876659276
PheGenI	rs876659276
Biobank	rs876659276
1000 genomes	rs876659276
hgdp	rs876659276
ensembl	rs876659276
geneview	rs876659276
scholar	rs876659276
google	rs876659276
pharmgkb	rs876659276
gwascentral	rs876659276
openSNP	rs876659276
23andMe	rs876659276
SNPshot	rs876659276
SNPdbe	rs876659276
MSV3d	rs876659276
GWAS Ctlg	rs876659276

Max Magnitude

6.2

ClinVar
Risk	rs876659276(A;A)
Alt	rs876659276(A;A)
Reference	Rs876659276(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHD
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.111965554T>A
CLNSRC
CLNACC	RCV000215839.1,