rs104894302

Orientation

plus

Stabilized

plus

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

Make rs104894302(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

112089002

Gene

SDHD

is a	snp
is	mentioned by
dbSNP	rs104894302
dbSNP (classic)	rs104894302
ClinGen	rs104894302
ebi	rs104894302
HLI	rs104894302
Exac	rs104894302
Gnomad	rs104894302
Varsome	rs104894302
LitVar	rs104894302
Map	rs104894302
PheGenI	rs104894302
Biobank	rs104894302
1000 genomes	rs104894302
hgdp	rs104894302
ensembl	rs104894302
geneview	rs104894302
scholar	rs104894302
google	rs104894302
pharmgkb	rs104894302
gwascentral	rs104894302
openSNP	rs104894302
23andMe	rs104894302
SNPshot	rs104894302
SNPdbe	rs104894302
MSV3d	rs104894302
GWAS Ctlg	rs104894302

Max Magnitude

6.2

OMIM	602690
Desc
Variant	0005
Related	also

ClinVar
Risk	rs104894302(G;G) rs104894302(T;T)
Alt	rs104894302(G;G) rs104894302(T;T)
Reference	Rs104894302(A;A)
Significance	Pathogenic
Disease	Paragangliomas 1
Variation	info
Gene	SDHD
CLNDBN	Paragangliomas 1
Reversed	0
HGVS	NC_000011.9:g.111959726A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007307.2,