rs863224065

Orientation

plus

Stabilized

plus

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

Make rs863224065(A;G)

Make rs863224065(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

11999004

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs863224065
dbSNP (classic)	rs863224065
ClinGen	rs863224065
ebi	rs863224065
HLI	rs863224065
Exac	rs863224065
Gnomad	rs863224065
Varsome	rs863224065
LitVar	rs863224065
Map	rs863224065
PheGenI	rs863224065
Biobank	rs863224065
1000 genomes	rs863224065
hgdp	rs863224065
ensembl	rs863224065
geneview	rs863224065
scholar	rs863224065
google	rs863224065
pharmgkb	rs863224065
gwascentral	rs863224065
openSNP	rs863224065
23andMe	rs863224065
SNPshot	rs863224065
SNPdbe	rs863224065
MSV3d	rs863224065
GWAS Ctlg	rs863224065

Max Magnitude

0

ClinVar
Risk	rs863224065(G;G)
Alt	rs863224065(G;G)
Reference	Rs863224065(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MFN2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.12059061A>G
CLNSRC
CLNACC	RCV000195514.1,