rs104894304

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	6.2	Hereditary PGL/PCC Syndrome

Make rs104894304(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

112094831

Gene

SDHD

is a	snp
is	mentioned by
dbSNP	rs104894304
dbSNP (classic)	rs104894304
ClinGen	rs104894304
ebi	rs104894304
HLI	rs104894304
Exac	rs104894304
Gnomad	rs104894304
Varsome	rs104894304
LitVar	rs104894304
Map	rs104894304
PheGenI	rs104894304
Biobank	rs104894304
1000 genomes	rs104894304
hgdp	rs104894304
ensembl	rs104894304
geneview	rs104894304
scholar	rs104894304
google	rs104894304
pharmgkb	rs104894304
gwascentral	rs104894304
openSNP	rs104894304
23andMe	rs104894304
SNPshot	rs104894304
SNPdbe	rs104894304
MSV3d	rs104894304
GWAS Ctlg	rs104894304

Max Magnitude

6.2

OMIM	602690
Desc
Variant	0007
Related	also

ClinVar
Risk	rs104894304(G;G)
Alt	rs104894304(G;G)
Reference	Rs104894304(A;A)
Significance	Pathogenic
Disease	Paragangliomas 1 Hereditary Paraganglioma-Pheochromocytoma Syndromes Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHD
CLNDBN	Paragangliomas 1 Hereditary Paraganglioma-Pheochromocytoma Syndromes Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.111965555A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007309.2, RCV000155750.1, RCV000221353.1,