rs774508076

Orientation

plus

Stabilized

plus

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

Make rs774508076(A;A)

Make rs774508076(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

61437753

Gene

SDHAF2

is a	snp
is	mentioned by
dbSNP	rs774508076
dbSNP (classic)	rs774508076
ClinGen	rs774508076
ebi	rs774508076
HLI	rs774508076
Exac	rs774508076
Gnomad	rs774508076
Varsome	rs774508076
LitVar	rs774508076
Map	rs774508076
PheGenI	rs774508076
Biobank	rs774508076
1000 genomes	rs774508076
hgdp	rs774508076
ensembl	rs774508076
geneview	rs774508076
scholar	rs774508076
google	rs774508076
pharmgkb	rs774508076
gwascentral	rs774508076
openSNP	rs774508076
23andMe	rs774508076
SNPshot	rs774508076
SNPdbe	rs774508076
MSV3d	rs774508076
GWAS Ctlg	rs774508076

Max Magnitude

0

ClinVar
Risk	rs774508076(A;A)
Alt	rs774508076(A;A)
Reference	Rs774508076(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SDHAF2
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.61205225G>A
CLNSRC
CLNACC	RCV000421747.1,