rs879253862

Orientation

plus

Stabilized

plus

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

Make rs879253862(A;A)

Make rs879253862(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

11997348

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs879253862
dbSNP (classic)	rs879253862
ClinGen	rs879253862
ebi	rs879253862
HLI	rs879253862
Exac	rs879253862
Gnomad	rs879253862
Varsome	rs879253862
LitVar	rs879253862
Map	rs879253862
PheGenI	rs879253862
Biobank	rs879253862
1000 genomes	rs879253862
hgdp	rs879253862
ensembl	rs879253862
geneview	rs879253862
scholar	rs879253862
google	rs879253862
pharmgkb	rs879253862
gwascentral	rs879253862
openSNP	rs879253862
23andMe	rs879253862
SNPshot	rs879253862
SNPdbe	rs879253862
MSV3d	rs879253862
GWAS Ctlg	rs879253862

Max Magnitude

0

ClinVar
Risk	rs879253862(A;A)
Alt	rs879253862(A;A)
Reference	Rs879253862(G;G)
Significance	Probable-Pathogenic
Disease	Charcot-Marie-Tooth disease
Variation	info
Gene	MFN2
CLNDBN	Charcot-Marie-Tooth disease, type 2A2
Reversed	0
HGVS	NC_000001.10:g.12057405G>A
CLNSRC
CLNACC	RCV000235058.1,