rs12069578

Orientation

plus

Stabilized

plus

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

Make rs12069578(A;A)

Make rs12069578(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

12004010

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs12069578
dbSNP (classic)	rs12069578
ClinGen	rs12069578
ebi	rs12069578
HLI	rs12069578
Exac	rs12069578
Gnomad	rs12069578
Varsome	rs12069578
LitVar	rs12069578
Map	rs12069578
PheGenI	rs12069578
Biobank	rs12069578
1000 genomes	rs12069578
hgdp	rs12069578
ensembl	rs12069578
geneview	rs12069578
scholar	rs12069578
google	rs12069578
pharmgkb	rs12069578
gwascentral	rs12069578
openSNP	rs12069578
23andMe	rs12069578
SNPshot	rs12069578
SNPdbe	rs12069578
MSV3d	rs12069578
GWAS Ctlg	rs12069578

Max Magnitude

0

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

ClinVar
Risk	rs12069578(A;A) rs12069578(C;C)
Alt	rs12069578(A;A) rs12069578(C;C)
Reference	Rs12069578(G;G)
Significance	Other
Disease	not specified
Variation	info
Gene	MFN2
CLNDBN	not specified
Reversed	0
HGVS	NC_000001.10:g.12064067G>A
CLNSRC
CLNACC	RCV000174373.5,