rs863224068

Orientation

plus

Stabilized

plus

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

Make rs863224068(G;T)

Make rs863224068(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

11992690

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs863224068
dbSNP (classic)	rs863224068
ClinGen	rs863224068
ebi	rs863224068
HLI	rs863224068
Exac	rs863224068
Gnomad	rs863224068
Varsome	rs863224068
LitVar	rs863224068
Map	rs863224068
PheGenI	rs863224068
Biobank	rs863224068
1000 genomes	rs863224068
hgdp	rs863224068
ensembl	rs863224068
geneview	rs863224068
scholar	rs863224068
google	rs863224068
pharmgkb	rs863224068
gwascentral	rs863224068
openSNP	rs863224068
23andMe	rs863224068
SNPshot	rs863224068
SNPdbe	rs863224068
MSV3d	rs863224068
GWAS Ctlg	rs863224068

Max Magnitude

0

ClinVar
Risk	rs863224068(T;T)
Alt	rs863224068(T;T)
Reference	Rs863224068(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MFN2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.12052747G>T
CLNSRC
CLNACC	RCV000196210.1,