rs786203457

Orientation

plus

Stabilized

plus

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

Make rs786203457(A;G)

Make rs786203457(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

161356815

Gene

SDHC

is a	snp
is	mentioned by
dbSNP	rs786203457
dbSNP (classic)	rs786203457
ClinGen	rs786203457
ebi	rs786203457
HLI	rs786203457
Exac	rs786203457
Gnomad	rs786203457
Varsome	rs786203457
LitVar	rs786203457
Map	rs786203457
PheGenI	rs786203457
Biobank	rs786203457
1000 genomes	rs786203457
hgdp	rs786203457
ensembl	rs786203457
geneview	rs786203457
scholar	rs786203457
google	rs786203457
pharmgkb	rs786203457
gwascentral	rs786203457
openSNP	rs786203457
23andMe	rs786203457
SNPshot	rs786203457
SNPdbe	rs786203457
MSV3d	rs786203457
GWAS Ctlg	rs786203457

Max Magnitude

0

ClinVar
Risk	rs786203457(G;G)
Alt	rs786203457(G;G)
Reference	Rs786203457(A;A)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	SDHC
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000001.10:g.161326605A>G
CLNSRC
CLNACC	RCV000166772.3, RCV000478217.1,