rs200095753

Orientation

plus

Stabilized

plus

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

Make rs200095753(C;T)

Make rs200095753(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

6300918

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs200095753
dbSNP (classic)	rs200095753
ClinGen	rs200095753
ebi	rs200095753
HLI	rs200095753
Exac	rs200095753
Gnomad	rs200095753
Varsome	rs200095753
LitVar	rs200095753
Map	rs200095753
PheGenI	rs200095753
Biobank	rs200095753
1000 genomes	rs200095753
hgdp	rs200095753
ensembl	rs200095753
geneview	rs200095753
scholar	rs200095753
google	rs200095753
pharmgkb	rs200095753
gwascentral	rs200095753
openSNP	rs200095753
23andMe	rs200095753
SNPshot	rs200095753
SNPdbe	rs200095753
MSV3d	rs200095753
GWAS Ctlg	rs200095753

Max Magnitude

0

ClinVar
Risk	rs200095753(A;A) rs200095753(T;T)
Alt	rs200095753(A;A) rs200095753(T;T)
Reference	Rs200095753(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	WFS1
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.6302645C>T
CLNSRC
CLNACC	RCV000196031.1,