rs876658486

Orientation

plus

Stabilized

plus

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

Make rs876658486(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

226041

Gene

SDHA

is a	snp
is	mentioned by
dbSNP	rs876658486
dbSNP (classic)	rs876658486
ClinGen	rs876658486
ebi	rs876658486
HLI	rs876658486
Exac	rs876658486
Gnomad	rs876658486
Varsome	rs876658486
LitVar	rs876658486
Map	rs876658486
PheGenI	rs876658486
Biobank	rs876658486
1000 genomes	rs876658486
hgdp	rs876658486
ensembl	rs876658486
geneview	rs876658486
scholar	rs876658486
google	rs876658486
pharmgkb	rs876658486
gwascentral	rs876658486
openSNP	rs876658486
23andMe	rs876658486
SNPshot	rs876658486
SNPdbe	rs876658486
MSV3d	rs876658486
GWAS Ctlg	rs876658486

Max Magnitude

6.2

ClinVar
Risk	rs876658486(A;A)
Alt	rs876658486(A;A)
Reference	Rs876658486(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHA
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.226156T>A
CLNSRC
CLNACC	RCV000221025.1,