rs138682654

Orientation

plus

Stabilized

plus

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

Make rs138682654(A;A)

Make rs138682654(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

6291367

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs138682654
dbSNP (classic)	rs138682654
ClinGen	rs138682654
ebi	rs138682654
HLI	rs138682654
Exac	rs138682654
Gnomad	rs138682654
Varsome	rs138682654
LitVar	rs138682654
Map	rs138682654
PheGenI	rs138682654
Biobank	rs138682654
1000 genomes	rs138682654
hgdp	rs138682654
ensembl	rs138682654
geneview	rs138682654
scholar	rs138682654
google	rs138682654
pharmgkb	rs138682654
gwascentral	rs138682654
openSNP	rs138682654
23andMe	rs138682654
SNPshot	rs138682654
SNPdbe	rs138682654
MSV3d	rs138682654
GWAS Ctlg	rs138682654

Max Magnitude

0

ClinVar
Risk	rs138682654(A;A)
Alt	rs138682654(A;A)
Reference	Rs138682654(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	WFS1
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.6293094G>A
CLNSRC
CLNACC	RCV000196477.1,