rs119103262

Orientation

plus

Stabilized

plus

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

Make rs119103262(C;G)

Make rs119103262(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11997315

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs119103262
dbSNP (classic)	rs119103262
ClinGen	rs119103262
ebi	rs119103262
HLI	rs119103262
Exac	rs119103262
Gnomad	rs119103262
Varsome	rs119103262
LitVar	rs119103262
Map	rs119103262
PheGenI	rs119103262
Biobank	rs119103262
1000 genomes	rs119103262
hgdp	rs119103262
ensembl	rs119103262
geneview	rs119103262
scholar	rs119103262
google	rs119103262
pharmgkb	rs119103262
gwascentral	rs119103262
openSNP	rs119103262
23andMe	rs119103262
SNPshot	rs119103262
SNPdbe	rs119103262
MSV3d	rs119103262
GWAS Ctlg	rs119103262

Max Magnitude

0

OMIM	608507
Desc
Variant	0008
Related	also

ClinVar
Risk	rs119103262(G;G)
Alt	rs119103262(G;G)
Reference	Rs119103262(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.12057372C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002363.5,