rs878854632

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CAG;CAG)	0	common in clinvar

Make rs878854632(-;-)

Make rs878854632(-;AGC)

Make rs878854632(AGC;AGC)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

225881

Gene

SDHA

is a	snp
is	mentioned by
dbSNP	rs878854632
dbSNP (classic)	rs878854632
ClinGen	rs878854632
ebi	rs878854632
HLI	rs878854632
Exac	rs878854632
Gnomad	rs878854632
Varsome	rs878854632
LitVar	rs878854632
Map	rs878854632
PheGenI	rs878854632
Biobank	rs878854632
1000 genomes	rs878854632
hgdp	rs878854632
ensembl	rs878854632
geneview	rs878854632
scholar	rs878854632
google	rs878854632
pharmgkb	rs878854632
gwascentral	rs878854632
openSNP	rs878854632
23andMe	rs878854632
SNPshot	rs878854632
SNPdbe	rs878854632
MSV3d	rs878854632
GWAS Ctlg	rs878854632

Max Magnitude

0

ClinVar
Risk	rs878854632(-;-)
Alt	rs878854632(-;-)
Reference	Rs878854632(CAG;CAG)
Significance	Probable-Pathogenic
Disease	Mitochondrial complex II deficiency Paragangliomas 5
Variation	info
Gene	SDHA
CLNDBN	Mitochondrial complex II deficiency Paragangliomas 5
Reversed	0
HGVS	NC_000005.9:g.225996_225998delAGC
CLNSRC
CLNACC	RCV000231881.2,