rs755235380

Orientation

plus

Stabilized

plus

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

Make rs755235380(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

161314406

Gene

SDHC

is a	snp
is	mentioned by
dbSNP	rs755235380
dbSNP (classic)	rs755235380
ClinGen	rs755235380
ebi	rs755235380
HLI	rs755235380
Exac	rs755235380
Gnomad	rs755235380
Varsome	rs755235380
LitVar	rs755235380
Map	rs755235380
PheGenI	rs755235380
Biobank	rs755235380
1000 genomes	rs755235380
hgdp	rs755235380
ensembl	rs755235380
geneview	rs755235380
scholar	rs755235380
google	rs755235380
pharmgkb	rs755235380
gwascentral	rs755235380
openSNP	rs755235380
23andMe	rs755235380
SNPshot	rs755235380
SNPdbe	rs755235380
MSV3d	rs755235380
GWAS Ctlg	rs755235380

Max Magnitude

6.2

ClinVar
Risk	rs755235380(G;G)
Alt	rs755235380(G;G)
Reference	Rs755235380(A;A)
Significance	Pathogenic
Disease	Paragangliomas 3 Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHC
CLNDBN	Paragangliomas 3 Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000001.10:g.161284196A>G
CLNSRC
CLNACC	RCV000467345.1, RCV000492170.1,