rs764575966

Orientation

plus

Stabilized

plus

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

Make rs764575966(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

161356832

Gene

SDHC

is a	snp
is	mentioned by
dbSNP	rs764575966
dbSNP (classic)	rs764575966
ClinGen	rs764575966
ebi	rs764575966
HLI	rs764575966
Exac	rs764575966
Gnomad	rs764575966
Varsome	rs764575966
LitVar	rs764575966
Map	rs764575966
PheGenI	rs764575966
Biobank	rs764575966
1000 genomes	rs764575966
hgdp	rs764575966
ensembl	rs764575966
geneview	rs764575966
scholar	rs764575966
google	rs764575966
pharmgkb	rs764575966
gwascentral	rs764575966
openSNP	rs764575966
23andMe	rs764575966
SNPshot	rs764575966
SNPdbe	rs764575966
MSV3d	rs764575966
GWAS Ctlg	rs764575966

Max Magnitude

6.2

ClinVar
Risk	rs764575966(T;T)
Alt	rs764575966(T;T)
Reference	Rs764575966(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Paragangliomas 3 not provided
Variation	info
Gene	SDHC
CLNDBN	Hereditary cancer-predisposing syndrome Paragangliomas 3 not provided
Reversed	0
HGVS	NC_000001.10:g.161326622C>T
CLNSRC
CLNACC	RCV000162467.3, RCV000232178.2, RCV000315495.2,