rs786202403

Orientation

plus

Stabilized

plus

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

Make rs786202403(A;A)

Make rs786202403(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

112089001

Gene

SDHD

is a	snp
is	mentioned by
dbSNP	rs786202403
dbSNP (classic)	rs786202403
ClinGen	rs786202403
ebi	rs786202403
HLI	rs786202403
Exac	rs786202403
Gnomad	rs786202403
Varsome	rs786202403
LitVar	rs786202403
Map	rs786202403
PheGenI	rs786202403
Biobank	rs786202403
1000 genomes	rs786202403
hgdp	rs786202403
ensembl	rs786202403
geneview	rs786202403
scholar	rs786202403
google	rs786202403
pharmgkb	rs786202403
gwascentral	rs786202403
openSNP	rs786202403
23andMe	rs786202403
SNPshot	rs786202403
SNPdbe	rs786202403
MSV3d	rs786202403
GWAS Ctlg	rs786202403

Max Magnitude

0

ClinVar
Risk	rs786202403(A;A)
Alt	rs786202403(A;A)
Reference	Rs786202403(C;C)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHD
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.111959725C>A
CLNSRC
CLNACC	RCV000165195.1,