rs104893883

Orientation

plus

Stabilized

plus

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

Make rs104893883(C;C)

Make rs104893883(C;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

6302281

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs104893883
dbSNP (classic)	rs104893883
ClinGen	rs104893883
ebi	rs104893883
HLI	rs104893883
Exac	rs104893883
Gnomad	rs104893883
Varsome	rs104893883
LitVar	rs104893883
Map	rs104893883
PheGenI	rs104893883
Biobank	rs104893883
1000 genomes	rs104893883
hgdp	rs104893883
ensembl	rs104893883
geneview	rs104893883
scholar	rs104893883
google	rs104893883
pharmgkb	rs104893883
gwascentral	rs104893883
openSNP	rs104893883
23andMe	rs104893883
SNPshot	rs104893883
SNPdbe	rs104893883
MSV3d	rs104893883
GWAS Ctlg	rs104893883

Max Magnitude

0

OMIM	606201
Desc
Variant	0015
Related	also

ClinVar
Risk	rs104893883(C;C)
Alt	rs104893883(C;C)
Reference	Rs104893883(T;T)
Significance	Pathogenic
Disease	WFS1-Related Disorders
Variation	info
Gene	WFS1
CLNDBN	WFS1-Related Disorders
Reversed	0
HGVS	NC_000004.11:g.6304008T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004779.3,