rs1801212

Orientation

plus

Stabilized

plus

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

Make rs1801212(A;A)

Make rs1801212(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

6300792

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs1801212
dbSNP (classic)	rs1801212
ClinGen	rs1801212
ebi	rs1801212
HLI	rs1801212
Exac	rs1801212
Gnomad	rs1801212
Varsome	rs1801212
LitVar	rs1801212
Map	rs1801212
PheGenI	rs1801212
Biobank	rs1801212
1000 genomes	rs1801212
hgdp	rs1801212
ensembl	rs1801212
geneview	rs1801212
scholar	rs1801212
google	rs1801212
pharmgkb	rs1801212
gwascentral	rs1801212
openSNP	rs1801212
23andMe	rs1801212
SNPshot	rs1801212
SNPdbe	rs1801212
MSV3d	rs1801212
GWAS Ctlg	rs1801212

GMAF

0.1364

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	rs1801212(A;A) rs1801212(T;T)
Alt	rs1801212(A;A) rs1801212(T;T)
Reference	Rs1801212(G;G)
Significance	Non-pathogenic
Disease	not specified WFS1-Related Spectrum Disorders
Variation	info
Gene	WFS1
CLNDBN	not specified WFS1-Related Spectrum Disorders
Reversed	0
HGVS	NC_000004.11:g.6302519G>A; NC_000004.11:g.6302519G>T
CLNSRC	HGMD UniProtKB (protein)
CLNACC	RCV000038668.8, RCV000259675.1, RCV000155337.1,