rs199910987

Orientation

plus

Stabilized

plus

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

Make rs199910987(A;A)

Make rs199910987(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

6301405

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs199910987
dbSNP (classic)	rs199910987
ClinGen	rs199910987
ebi	rs199910987
HLI	rs199910987
Exac	rs199910987
Gnomad	rs199910987
Varsome	rs199910987
LitVar	rs199910987
Map	rs199910987
PheGenI	rs199910987
Biobank	rs199910987
1000 genomes	rs199910987
hgdp	rs199910987
ensembl	rs199910987
geneview	rs199910987
scholar	rs199910987
google	rs199910987
pharmgkb	rs199910987
gwascentral	rs199910987
openSNP	rs199910987
23andMe	rs199910987
SNPshot	rs199910987
SNPdbe	rs199910987
MSV3d	rs199910987
GWAS Ctlg	rs199910987

Max Magnitude

0

ClinVar
Risk	rs199910987(A;A)
Alt	rs199910987(A;A)
Reference	Rs199910987(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	WFS1
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.6303132G>A
CLNSRC
CLNACC	RCV000200051.2,