rs587776647

Orientation

plus

Stabilized

plus

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

Make rs587776647(-;-)

Reference

GRCh38 38.1/142

Chromosome

11

Position

112094953

Gene

SDHD

is a	snp
is	mentioned by
dbSNP	rs587776647
dbSNP (classic)	rs587776647
ClinGen	rs587776647
ebi	rs587776647
HLI	rs587776647
Exac	rs587776647
Gnomad	rs587776647
Varsome	rs587776647
LitVar	rs587776647
Map	rs587776647
PheGenI	rs587776647
Biobank	rs587776647
1000 genomes	rs587776647
hgdp	rs587776647
ensembl	rs587776647
geneview	rs587776647
scholar	rs587776647
google	rs587776647
pharmgkb	rs587776647
gwascentral	rs587776647
openSNP	rs587776647
23andMe	rs587776647
SNPshot	rs587776647
SNPdbe	rs587776647
MSV3d	rs587776647
GWAS Ctlg	rs587776647

Max Magnitude

6.2

ClinVar
Risk	rs587776647(-;-)
Alt	rs587776647(-;-)
Reference	Rs587776647(A;A)
Significance	Pathogenic
Disease	Paragangliomas 1
Variation	info
Gene	SDHD
CLNDBN	Paragangliomas 1
Reversed	0
HGVS	NC_000011.9:g.111965677delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007319.2,