rs369762154

Orientation

plus

Stabilized

plus

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

Make rs369762154(C;T)

Make rs369762154(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

12007167

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs369762154
dbSNP (classic)	rs369762154
ClinGen	rs369762154
ebi	rs369762154
HLI	rs369762154
Exac	rs369762154
Gnomad	rs369762154
Varsome	rs369762154
LitVar	rs369762154
Map	rs369762154
PheGenI	rs369762154
Biobank	rs369762154
1000 genomes	rs369762154
hgdp	rs369762154
ensembl	rs369762154
geneview	rs369762154
scholar	rs369762154
google	rs369762154
pharmgkb	rs369762154
gwascentral	rs369762154
openSNP	rs369762154
23andMe	rs369762154
SNPshot	rs369762154
SNPdbe	rs369762154
MSV3d	rs369762154
GWAS Ctlg	rs369762154

Max Magnitude

0

ClinVar
Risk	rs369762154(G;G) rs369762154(T;T)
Alt	rs369762154(G;G) rs369762154(T;T)
Reference	Rs369762154(C;C)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MFN2
CLNDBN	not specified
Reversed	0
HGVS	NC_000001.10:g.12067224C>T
CLNSRC
CLNACC	RCV000197786.3,