rs863224064

Orientation

plus

Stabilized

plus

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

Make rs863224064(A;A)

Make rs863224064(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

11997363

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs863224064
dbSNP (classic)	rs863224064
ClinGen	rs863224064
ebi	rs863224064
HLI	rs863224064
Exac	rs863224064
Gnomad	rs863224064
Varsome	rs863224064
LitVar	rs863224064
Map	rs863224064
PheGenI	rs863224064
Biobank	rs863224064
1000 genomes	rs863224064
hgdp	rs863224064
ensembl	rs863224064
geneview	rs863224064
scholar	rs863224064
google	rs863224064
pharmgkb	rs863224064
gwascentral	rs863224064
openSNP	rs863224064
23andMe	rs863224064
SNPshot	rs863224064
SNPdbe	rs863224064
MSV3d	rs863224064
GWAS Ctlg	rs863224064

Max Magnitude

0

ClinVar
Risk	rs863224064(A;A)
Alt	rs863224064(A;A)
Reference	Rs863224064(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MFN2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.12057420G>A
CLNSRC
CLNACC	RCV000199084.2,