rs397517196

Orientation

plus

Stabilized

plus

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

Make rs397517196(A;C)

Make rs397517196(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

6301936

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs397517196
dbSNP (classic)	rs397517196
ClinGen	rs397517196
ebi	rs397517196
HLI	rs397517196
Exac	rs397517196
Gnomad	rs397517196
Varsome	rs397517196
LitVar	rs397517196
Map	rs397517196
PheGenI	rs397517196
Biobank	rs397517196
1000 genomes	rs397517196
hgdp	rs397517196
ensembl	rs397517196
geneview	rs397517196
scholar	rs397517196
google	rs397517196
pharmgkb	rs397517196
gwascentral	rs397517196
openSNP	rs397517196
23andMe	rs397517196
SNPshot	rs397517196
SNPdbe	rs397517196
MSV3d	rs397517196
GWAS Ctlg	rs397517196

Max Magnitude

0

ClinVar
Risk	rs397517196(C;C)
Alt	rs397517196(C;C)
Reference	Rs397517196(A;A)
Significance	Pathogenic
Disease	WFS1-Related Disorders
Variation	info
Gene	WFS1
CLNDBN	WFS1-Related Disorders
Reversed	0
HGVS	NC_000004.11:g.6303663A>C
CLNSRC
CLNACC	RCV000038651.2,