rs587776598

Orientation

plus

Stabilized

plus

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

Make rs587776598(-;GGCCGTCGCGAGGCTG)

Make rs587776598(GGCCGTCGCGAGGCTG;GGCCGTCGCGAGGCTG)

Reference

GRCh38 38.1/142

Chromosome

4

Position

6289095

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs587776598
dbSNP (classic)	rs587776598
ClinGen	rs587776598
ebi	rs587776598
HLI	rs587776598
Exac	rs587776598
Gnomad	rs587776598
Varsome	rs587776598
LitVar	rs587776598
Map	rs587776598
PheGenI	rs587776598
Biobank	rs587776598
1000 genomes	rs587776598
hgdp	rs587776598
ensembl	rs587776598
geneview	rs587776598
scholar	rs587776598
google	rs587776598
pharmgkb	rs587776598
gwascentral	rs587776598
openSNP	rs587776598
23andMe	rs587776598
SNPshot	rs587776598
SNPdbe	rs587776598
MSV3d	rs587776598
GWAS Ctlg	rs587776598

Max Magnitude

0

ClinVar
Risk	rs587776598(GGCCGTCGCGAGGCTG;GGCCGTCGCGAGGCTG) rs587776598(GGGCCGTCGCGAGGCT;GGGCCGTCGCGAGGCT)
Alt	rs587776598(GGCCGTCGCGAGGCTG;GGCCGTCGCGAGGCTG) rs587776598(GGGCCGTCGCGAGGCT;GGGCCGTCGCGAGGCT)
Reference	Rs587776598(-;-)
Significance	Pathogenic
Disease	Diabetes mellitus AND insipidus with optic atrophy AND deafness
Variation	info
Gene	WFS1
CLNDBN	Diabetes mellitus AND insipidus with optic atrophy AND deafness
Reversed	0
HGVS	NC_000004.11:g.6290807_6290822dup16
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004777.4,