rs786203932

Orientation

plus

Stabilized

plus

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

Make rs786203932(A;A)

Make rs786203932(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

112094902

Gene

SDHD

is a	snp
is	mentioned by
dbSNP	rs786203932
dbSNP (classic)	rs786203932
ClinGen	rs786203932
ebi	rs786203932
HLI	rs786203932
Exac	rs786203932
Gnomad	rs786203932
Varsome	rs786203932
LitVar	rs786203932
Map	rs786203932
PheGenI	rs786203932
Biobank	rs786203932
1000 genomes	rs786203932
hgdp	rs786203932
ensembl	rs786203932
geneview	rs786203932
scholar	rs786203932
google	rs786203932
pharmgkb	rs786203932
gwascentral	rs786203932
openSNP	rs786203932
23andMe	rs786203932
SNPshot	rs786203932
SNPdbe	rs786203932
MSV3d	rs786203932
GWAS Ctlg	rs786203932

Max Magnitude

0

ClinVar
Risk	rs786203932(A;A)
Alt	rs786203932(A;A)
Reference	Rs786203932(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	SDHD
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.111965626G>A
CLNSRC
CLNACC	RCV000167450.2, RCV000478572.1,