rs869312963

Orientation

minus

Stabilized

minus

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

Make rs869312963(C;C)

Make rs869312963(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

9816961

Gene

SBF2

is a	snp
is	mentioned by
dbSNP	rs869312963
dbSNP (classic)	rs869312963
ClinGen	rs869312963
ebi	rs869312963
HLI	rs869312963
Exac	rs869312963
Gnomad	rs869312963
Varsome	rs869312963
LitVar	rs869312963
Map	rs869312963
PheGenI	rs869312963
Biobank	rs869312963
1000 genomes	rs869312963
hgdp	rs869312963
ensembl	rs869312963
geneview	rs869312963
scholar	rs869312963
google	rs869312963
pharmgkb	rs869312963
gwascentral	rs869312963
openSNP	rs869312963
23andMe	rs869312963
SNPshot	rs869312963
SNPdbe	rs869312963
MSV3d	rs869312963
GWAS Ctlg	rs869312963

Max Magnitude

0

ClinVar
Risk	rs869312963(C;C)
Alt	rs869312963(C;C)
Reference	Rs869312963(T;T)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	SBF2
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000011.9:g.9838508A>G
CLNSRC
CLNACC	RCV000210630.1,