rs143064649

Orientation

plus

Stabilized

plus

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

Make rs143064649(A;A)

Make rs143064649(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

4

Position

6301634

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs143064649
dbSNP (classic)	rs143064649
ClinGen	rs143064649
ebi	rs143064649
HLI	rs143064649
Exac	rs143064649
Gnomad	rs143064649
Varsome	rs143064649
LitVar	rs143064649
Map	rs143064649
PheGenI	rs143064649
Biobank	rs143064649
1000 genomes	rs143064649
hgdp	rs143064649
ensembl	rs143064649
geneview	rs143064649
scholar	rs143064649
google	rs143064649
pharmgkb	rs143064649
gwascentral	rs143064649
openSNP	rs143064649
23andMe	rs143064649
SNPshot	rs143064649
SNPdbe	rs143064649
MSV3d	rs143064649
GWAS Ctlg	rs143064649

Max Magnitude

0

ClinVar
Risk	rs143064649(A;A)
Alt	rs143064649(A;A)
Reference	Rs143064649(G;G)
Significance	Probable-Pathogenic
Disease	WFS1-Related Spectrum Disorders
Variation	info
Gene	WFS1
CLNDBN	WFS1-Related Spectrum Disorders
Reversed	0
HGVS	NC_000004.11:g.6303361G>A
CLNSRC	Illumina
CLNACC	RCV000285512.1,