rs794729198

Orientation

plus

Stabilized

plus

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

Make rs794729198(C;T)

Make rs794729198(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

11999025

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs794729198
dbSNP (classic)	rs794729198
ClinGen	rs794729198
ebi	rs794729198
HLI	rs794729198
Exac	rs794729198
Gnomad	rs794729198
Varsome	rs794729198
LitVar	rs794729198
Map	rs794729198
PheGenI	rs794729198
Biobank	rs794729198
1000 genomes	rs794729198
hgdp	rs794729198
ensembl	rs794729198
geneview	rs794729198
scholar	rs794729198
google	rs794729198
pharmgkb	rs794729198
gwascentral	rs794729198
openSNP	rs794729198
23andMe	rs794729198
SNPshot	rs794729198
SNPdbe	rs794729198
MSV3d	rs794729198
GWAS Ctlg	rs794729198

Max Magnitude

0

ClinVar
Risk	rs794729198(T;T)
Alt	rs794729198(T;T)
Reference	Rs794729198(C;C)
Significance	Pathogenic
Disease	Charcot-Marie-Tooth disease
Variation	info
Gene	MFN2
CLNDBN	Charcot-Marie-Tooth disease, type 2A2
Reversed	0
HGVS	NC_000001.10:g.12059082C>T
CLNSRC
CLNACC	RCV000184017.1,