rs201286421

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs201286421(C;T)

Make rs201286421(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

161323636

Gene

SDHC

is a	snp
is	mentioned by
dbSNP	rs201286421
dbSNP (classic)	rs201286421
ClinGen	rs201286421
ebi	rs201286421
HLI	rs201286421
Exac	rs201286421
Gnomad	rs201286421
Varsome	rs201286421
LitVar	rs201286421
Map	rs201286421
PheGenI	rs201286421
Biobank	rs201286421
1000 genomes	rs201286421
hgdp	rs201286421
ensembl	rs201286421
geneview	rs201286421
scholar	rs201286421
google	rs201286421
pharmgkb	rs201286421
gwascentral	rs201286421
openSNP	rs201286421
23andMe	rs201286421
SNPshot	rs201286421
SNPdbe	rs201286421
MSV3d	rs201286421
GWAS Ctlg	rs201286421

Max Magnitude

0

ClinVar
Risk	rs201286421(T;T)
Alt	rs201286421(T;T)
Reference	Rs201286421(C;C)
Significance	Pathogenic
Disease	Paragangliomas 3 Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	SDHC
CLNDBN	Paragangliomas 3 Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000001.10:g.161293426C>T
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000034695.2, RCV000128874.4, RCV000486068.1,