rs786202200

Orientation

plus

Stabilized

plus

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

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

161328395

Gene

SDHC

is a	snp
is	mentioned by
dbSNP	rs786202200
dbSNP (classic)	rs786202200
ClinGen	rs786202200
ebi	rs786202200
HLI	rs786202200
Exac	rs786202200
Gnomad	rs786202200
Varsome	rs786202200
LitVar	rs786202200
Map	rs786202200
PheGenI	rs786202200
Biobank	rs786202200
1000 genomes	rs786202200
hgdp	rs786202200
ensembl	rs786202200
geneview	rs786202200
scholar	rs786202200
google	rs786202200
pharmgkb	rs786202200
gwascentral	rs786202200
openSNP	rs786202200
23andMe	rs786202200
SNPshot	rs786202200
SNPdbe	rs786202200
MSV3d	rs786202200
GWAS Ctlg	rs786202200

Max Magnitude

6.2

ClinVar
Risk	Rs786202200(A;A)
Alt	Rs786202200(A;A)
Reference	Rs786202200(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHC
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000001.10:g.161298185G>A
CLNSRC
CLNACC	RCV000164903.1,