rs869312970

Orientation

minus

Stabilized

minus

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

Make rs869312970(A;G)

Make rs869312970(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

9832274

Gene

SBF2

is a	snp
is	mentioned by
dbSNP	rs869312970
dbSNP (classic)	rs869312970
ClinGen	rs869312970
ebi	rs869312970
HLI	rs869312970
Exac	rs869312970
Gnomad	rs869312970
Varsome	rs869312970
LitVar	rs869312970
Map	rs869312970
PheGenI	rs869312970
Biobank	rs869312970
1000 genomes	rs869312970
hgdp	rs869312970
ensembl	rs869312970
geneview	rs869312970
scholar	rs869312970
google	rs869312970
pharmgkb	rs869312970
gwascentral	rs869312970
openSNP	rs869312970
23andMe	rs869312970
SNPshot	rs869312970
SNPdbe	rs869312970
MSV3d	rs869312970
GWAS Ctlg	rs869312970

Max Magnitude

0

ClinVar
Risk	rs869312970(G;G)
Alt	rs869312970(G;G)
Reference	Rs869312970(A;A)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	SBF2
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000011.9:g.9853821T>C
CLNSRC
CLNACC	RCV000210731.1,