rs587777112

Orientation

plus

Stabilized

plus

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

Make rs587777112(-;C)

Make rs587777112(C;C)

Reference

GRCh38 38.1/142

Chromosome

3

Position

184357432

Gene

CLCN2

is a	snp
is	mentioned by
dbSNP	rs587777112
dbSNP (classic)	rs587777112
ClinGen	rs587777112
ebi	rs587777112
HLI	rs587777112
Exac	rs587777112
Gnomad	rs587777112
Varsome	rs587777112
LitVar	rs587777112
Map	rs587777112
PheGenI	rs587777112
Biobank	rs587777112
1000 genomes	rs587777112
hgdp	rs587777112
ensembl	rs587777112
geneview	rs587777112
scholar	rs587777112
google	rs587777112
pharmgkb	rs587777112
gwascentral	rs587777112
openSNP	rs587777112
23andMe	rs587777112
SNPshot	rs587777112
SNPdbe	rs587777112
MSV3d	rs587777112
GWAS Ctlg	rs587777112

Max Magnitude

0

ClinVar
Risk	rs587777112(C;C)
Alt	rs587777112(C;C)
Reference	Rs587777112(-;-)
Significance	Pathogenic
Disease	Leukoencephalopathy with ataxia
Variation	info
Gene	CLCN2
CLNDBN	Leukoencephalopathy with ataxia
Reversed	0
HGVS	NC_000003.11:g.184075220dupC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000087032.4,