rs753237278

Orientation

plus

Stabilized

plus

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

Make rs753237278(A;A)

Make rs753237278(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

6301479

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs753237278
dbSNP (classic)	rs753237278
ClinGen	rs753237278
ebi	rs753237278
HLI	rs753237278
Exac	rs753237278
Gnomad	rs753237278
Varsome	rs753237278
LitVar	rs753237278
Map	rs753237278
PheGenI	rs753237278
Biobank	rs753237278
1000 genomes	rs753237278
hgdp	rs753237278
ensembl	rs753237278
geneview	rs753237278
scholar	rs753237278
google	rs753237278
pharmgkb	rs753237278
gwascentral	rs753237278
openSNP	rs753237278
23andMe	rs753237278
SNPshot	rs753237278
SNPdbe	rs753237278
MSV3d	rs753237278
GWAS Ctlg	rs753237278

Max Magnitude

0

ClinVar
Risk	rs753237278(A;A) rs753237278(C;C)
Alt	rs753237278(A;A) rs753237278(C;C)
Reference	Rs753237278(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	WFS1
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.6303206G>C
CLNSRC
CLNACC	RCV000198315.3,