rs876658350

Orientation

plus

Stabilized

plus

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

Make rs876658350(A;A)

Make rs876658350(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

61438090

Gene

SDHAF2

is a	snp
is	mentioned by
dbSNP	rs876658350
dbSNP (classic)	rs876658350
ClinGen	rs876658350
ebi	rs876658350
HLI	rs876658350
Exac	rs876658350
Gnomad	rs876658350
Varsome	rs876658350
LitVar	rs876658350
Map	rs876658350
PheGenI	rs876658350
Biobank	rs876658350
1000 genomes	rs876658350
hgdp	rs876658350
ensembl	rs876658350
geneview	rs876658350
scholar	rs876658350
google	rs876658350
pharmgkb	rs876658350
gwascentral	rs876658350
openSNP	rs876658350
23andMe	rs876658350
SNPshot	rs876658350
SNPdbe	rs876658350
MSV3d	rs876658350
GWAS Ctlg	rs876658350

Max Magnitude

0

ClinVar
Risk	rs876658350(A;A)
Alt	rs876658350(A;A)
Reference	Rs876658350(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHAF2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.61205562G>A
CLNSRC
CLNACC	RCV000213784.1,