rs587776652

Orientation

plus

Stabilized

plus

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

Make rs587776652(A;A)

Reference

GRCh38 38.1/142

Chromosome

1

Position

161314408

Gene

SDHC

is a	snp
is	mentioned by
dbSNP	rs587776652
dbSNP (classic)	rs587776652
ClinGen	rs587776652
ebi	rs587776652
HLI	rs587776652
Exac	rs587776652
Gnomad	rs587776652
Varsome	rs587776652
LitVar	rs587776652
Map	rs587776652
PheGenI	rs587776652
Biobank	rs587776652
1000 genomes	rs587776652
hgdp	rs587776652
ensembl	rs587776652
geneview	rs587776652
scholar	rs587776652
google	rs587776652
pharmgkb	rs587776652
gwascentral	rs587776652
openSNP	rs587776652
23andMe	rs587776652
SNPshot	rs587776652
SNPdbe	rs587776652
MSV3d	rs587776652
GWAS Ctlg	rs587776652

Max Magnitude

6.2

ClinVar
Risk	rs587776652(A;A)
Alt	rs587776652(A;A)
Reference	Rs587776652(G;G)
Significance	Pathogenic
Disease	Paragangliomas 3
Variation	info
Gene	SDHC
CLNDBN	Paragangliomas 3
Reversed	0
HGVS	NC_000001.10:g.161284198G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007663.4,