rs587776648

Orientation

plus

Stabilized

plus

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

Make rs587776648(-;-)

Make rs587776648(GACT;GACT)

Reference

GRCh38 38.1/142

Chromosome

11

Position

112094827

Gene

SDHD

is a	snp
is	mentioned by
dbSNP	rs587776648
dbSNP (classic)	rs587776648
ClinGen	rs587776648
ebi	rs587776648
HLI	rs587776648
Exac	rs587776648
Gnomad	rs587776648
Varsome	rs587776648
LitVar	rs587776648
Map	rs587776648
PheGenI	rs587776648
Biobank	rs587776648
1000 genomes	rs587776648
hgdp	rs587776648
ensembl	rs587776648
geneview	rs587776648
scholar	rs587776648
google	rs587776648
pharmgkb	rs587776648
gwascentral	rs587776648
openSNP	rs587776648
23andMe	rs587776648
SNPshot	rs587776648
SNPdbe	rs587776648
MSV3d	rs587776648
GWAS Ctlg	rs587776648

Max Magnitude

6.2

ClinVar
Risk	rs587776648(-;-)
Alt	rs587776648(-;-)
Reference	Rs587776648(ACTG;ACTG)
Significance	Pathogenic
Disease	Paragangliomas 1 not provided
Variation	info
Gene	SDHD
CLNDBN	Paragangliomas 1 not provided
Reversed	0
HGVS	NC_000011.9:g.111965551_111965554delGACT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007321.2, RCV000485947.1,