rs119103261

Orientation

plus

Stabilized

plus

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

Make rs119103261(C;C)

Make rs119103261(C;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

12002014

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs119103261
dbSNP (classic)	rs119103261
ClinGen	rs119103261
ebi	rs119103261
HLI	rs119103261
Exac	rs119103261
Gnomad	rs119103261
Varsome	rs119103261
LitVar	rs119103261
Map	rs119103261
PheGenI	rs119103261
Biobank	rs119103261
1000 genomes	rs119103261
hgdp	rs119103261
ensembl	rs119103261
geneview	rs119103261
scholar	rs119103261
google	rs119103261
pharmgkb	rs119103261
gwascentral	rs119103261
openSNP	rs119103261
23andMe	rs119103261
SNPshot	rs119103261
SNPdbe	rs119103261
MSV3d	rs119103261
GWAS Ctlg	rs119103261

Max Magnitude

0

OMIM	608507
Desc
Variant	0007
Related	also

ClinVar
Risk	rs119103261(C;C)
Alt	rs119103261(C;C)
Reference	Rs119103261(G;G)
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.12062071G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002362.3,