rs863224066

Orientation

plus

Stabilized

plus

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

Make rs863224066(C;T)

Make rs863224066(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

12001482

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs863224066
dbSNP (classic)	rs863224066
ClinGen	rs863224066
ebi	rs863224066
HLI	rs863224066
Exac	rs863224066
Gnomad	rs863224066
Varsome	rs863224066
LitVar	rs863224066
Map	rs863224066
PheGenI	rs863224066
Biobank	rs863224066
1000 genomes	rs863224066
hgdp	rs863224066
ensembl	rs863224066
geneview	rs863224066
scholar	rs863224066
google	rs863224066
pharmgkb	rs863224066
gwascentral	rs863224066
openSNP	rs863224066
23andMe	rs863224066
SNPshot	rs863224066
SNPdbe	rs863224066
MSV3d	rs863224066
GWAS Ctlg	rs863224066

Max Magnitude

0

ClinVar
Risk	rs863224066(T;T)
Alt	rs863224066(T;T)
Reference	Rs863224066(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MFN2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.12061539C>T
CLNSRC
CLNACC	RCV000195483.2,