rs1060501925

Orientation

plus

Stabilized

plus

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

Make rs1060501925(G;T)

Make rs1060501925(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

12011511

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs1060501925
dbSNP (classic)	rs1060501925
ClinGen	rs1060501925
ebi	rs1060501925
HLI	rs1060501925
Exac	rs1060501925
Gnomad	rs1060501925
Varsome	rs1060501925
LitVar	rs1060501925
Map	rs1060501925
PheGenI	rs1060501925
Biobank	rs1060501925
1000 genomes	rs1060501925
hgdp	rs1060501925
ensembl	rs1060501925
geneview	rs1060501925
scholar	rs1060501925
google	rs1060501925
pharmgkb	rs1060501925
gwascentral	rs1060501925
openSNP	rs1060501925
23andMe	rs1060501925
SNPshot	rs1060501925
SNPdbe	rs1060501925
MSV3d	rs1060501925
GWAS Ctlg	rs1060501925

Max Magnitude

0

ClinVar
Risk	rs1060501925(T;T)
Alt	rs1060501925(T;T)
Reference	Rs1060501925(G;G)
Significance	Probable-Pathogenic
Disease	Charcot-Marie-Tooth disease
Variation	info
Gene	MFN2
CLNDBN	Charcot-Marie-Tooth disease, type 2
Reversed	0
HGVS	NC_000001.10:g.12071568G>T
CLNSRC
CLNACC	RCV000458069.1,