rs587778661

Orientation

plus

Stabilized

plus

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

Make rs587778661(C;T)

Make rs587778661(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

161328466

Gene

SDHC

is a	snp
is	mentioned by
dbSNP	rs587778661
dbSNP (classic)	rs587778661
ClinGen	rs587778661
ebi	rs587778661
HLI	rs587778661
Exac	rs587778661
Gnomad	rs587778661
Varsome	rs587778661
LitVar	rs587778661
Map	rs587778661
PheGenI	rs587778661
Biobank	rs587778661
1000 genomes	rs587778661
hgdp	rs587778661
ensembl	rs587778661
geneview	rs587778661
scholar	rs587778661
google	rs587778661
pharmgkb	rs587778661
gwascentral	rs587778661
openSNP	rs587778661
23andMe	rs587778661
SNPshot	rs587778661
SNPdbe	rs587778661
MSV3d	rs587778661
GWAS Ctlg	rs587778661

Max Magnitude

0

ClinVar
Risk	rs587778661(T;T)
Alt	rs587778661(T;T)
Reference	Rs587778661(C;C)
Significance	Probable-Pathogenic
Disease	not specified Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHC
CLNDBN	not specified Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000001.10:g.161298256C>T
CLNSRC
CLNACC	RCV000122003.1, RCV000492504.1,