rs145639028

Orientation

plus

Stabilized

plus

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

Make rs145639028(A;A)

Make rs145639028(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

6289047

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs145639028
dbSNP (classic)	rs145639028
ClinGen	rs145639028
ebi	rs145639028
HLI	rs145639028
Exac	rs145639028
Gnomad	rs145639028
Varsome	rs145639028
LitVar	rs145639028
Map	rs145639028
PheGenI	rs145639028
Biobank	rs145639028
1000 genomes	rs145639028
hgdp	rs145639028
ensembl	rs145639028
geneview	rs145639028
scholar	rs145639028
google	rs145639028
pharmgkb	rs145639028
gwascentral	rs145639028
openSNP	rs145639028
23andMe	rs145639028
SNPshot	rs145639028
SNPdbe	rs145639028
MSV3d	rs145639028
GWAS Ctlg	rs145639028

Max Magnitude

0

ClinVar
Risk	rs145639028(A;A)
Alt	rs145639028(A;A)
Reference	Rs145639028(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	WFS1
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.6290774G>A
CLNSRC
CLNACC	RCV000413912.1,