rs1341667

Orientation

minus

Stabilized

minus

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

Make rs1341667(A;G)

Make rs1341667(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

68882104

Gene

STOX1

is a	snp
is	mentioned by
dbSNP	rs1341667
dbSNP (classic)	rs1341667
ClinGen	rs1341667
ebi	rs1341667
HLI	rs1341667
Exac	rs1341667
Gnomad	rs1341667
Varsome	rs1341667
LitVar	rs1341667
Map	rs1341667
PheGenI	rs1341667
Biobank	rs1341667
1000 genomes	rs1341667
hgdp	rs1341667
ensembl	rs1341667
geneview	rs1341667
scholar	rs1341667
google	rs1341667
pharmgkb	rs1341667
gwascentral	rs1341667
openSNP	rs1341667
23andMe	rs1341667
SNPshot	rs1341667
SNPdbe	rs1341667
MSV3d	rs1341667
GWAS Ctlg	rs1341667

GMAF

0.3673

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

OMIM	609397
Desc
Variant	0001
Related	also

ClinVar
Risk	rs1341667(G;G)
Alt	rs1341667(G;G)
Reference	Rs1341667(A;A)
Significance	Other
Disease	Preeclampsia/eclampsia 4
Variation	info
Gene	STOX1
CLNDBN	Preeclampsia/eclampsia 4
Reversed	1
HGVS	NC_000010.10:g.70641860T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001789.1,

[PMID 16385451] A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.