rs797046112

Orientation

plus

Stabilized

plus

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

Make rs797046112(-;-)

Make rs797046112(-;TTC)

Make rs797046112(TTC;TTC)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

6301035

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs797046112
dbSNP (classic)	rs797046112
ClinGen	rs797046112
ebi	rs797046112
HLI	rs797046112
Exac	rs797046112
Gnomad	rs797046112
Varsome	rs797046112
LitVar	rs797046112
Map	rs797046112
PheGenI	rs797046112
Biobank	rs797046112
1000 genomes	rs797046112
hgdp	rs797046112
ensembl	rs797046112
geneview	rs797046112
scholar	rs797046112
google	rs797046112
pharmgkb	rs797046112
gwascentral	rs797046112
openSNP	rs797046112
23andMe	rs797046112
SNPshot	rs797046112
SNPdbe	rs797046112
MSV3d	rs797046112
GWAS Ctlg	rs797046112

Max Magnitude

0

ClinVar
Risk	rs797046112(-;-)
Alt	rs797046112(-;-)
Reference	Rs797046112(TCT;TCT)
Significance	Probable-Pathogenic
Disease	Wolfram syndrome
Variation	info
Gene	WFS1
CLNDBN	Wolfram syndrome
Reversed	0
HGVS	NC_000004.11:g.6302762_6302764delTTC
CLNSRC
CLNACC	RCV000193337.1,