rs387906655

Orientation

plus

Stabilized

plus

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

Make rs387906655(C;G)

Make rs387906655(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

29659628

Gene

MOG

is a	snp
is	mentioned by
dbSNP	rs387906655
dbSNP (classic)	rs387906655
ClinGen	rs387906655
ebi	rs387906655
HLI	rs387906655
Exac	rs387906655
Gnomad	rs387906655
Varsome	rs387906655
LitVar	rs387906655
Map	rs387906655
PheGenI	rs387906655
Biobank	rs387906655
1000 genomes	rs387906655
hgdp	rs387906655
ensembl	rs387906655
geneview	rs387906655
scholar	rs387906655
google	rs387906655
pharmgkb	rs387906655
gwascentral	rs387906655
openSNP	rs387906655
23andMe	rs387906655
SNPshot	rs387906655
SNPdbe	rs387906655
MSV3d	rs387906655
GWAS Ctlg	rs387906655

Max Magnitude

0

ClinVar
Risk	rs387906655(G;G)
Alt	rs387906655(G;G)
Reference	Rs387906655(C;C)
Significance	Pathogenic
Disease	Narcolepsy 7
Variation	info
Gene	MOG
CLNDBN	Narcolepsy 7
Reversed	0
HGVS	NC_000006.11:g.29627405C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000022667.26,