rs587776645

Orientation

plus

Stabilized

plus

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

Make rs587776645(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

112094827

Gene

SDHD

is a	snp
is	mentioned by
dbSNP	rs587776645
dbSNP (classic)	rs587776645
ClinGen	rs587776645
ebi	rs587776645
HLI	rs587776645
Exac	rs587776645
Gnomad	rs587776645
Varsome	rs587776645
LitVar	rs587776645
Map	rs587776645
PheGenI	rs587776645
Biobank	rs587776645
1000 genomes	rs587776645
hgdp	rs587776645
ensembl	rs587776645
geneview	rs587776645
scholar	rs587776645
google	rs587776645
pharmgkb	rs587776645
gwascentral	rs587776645
openSNP	rs587776645
23andMe	rs587776645
SNPshot	rs587776645
SNPdbe	rs587776645
MSV3d	rs587776645
GWAS Ctlg	rs587776645

Max Magnitude

6.2

ClinVar
Risk	rs587776645(T;T)
Alt	rs587776645(T;T)
Reference	Rs587776645(-;-)
Significance	Pathogenic
Disease	Paragangliomas 1
Variation	info
Gene	SDHD
CLNDBN	Paragangliomas 1
Reversed	0
HGVS	NC_000011.9:g.111965551_111965552insT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007308.2,