rs119103266

Orientation

plus

Stabilized

plus

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

Make rs119103266(C;T)

Make rs119103266(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11998787

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs119103266
dbSNP (classic)	rs119103266
ClinGen	rs119103266
ebi	rs119103266
HLI	rs119103266
Exac	rs119103266
Gnomad	rs119103266
Varsome	rs119103266
LitVar	rs119103266
Map	rs119103266
PheGenI	rs119103266
Biobank	rs119103266
1000 genomes	rs119103266
hgdp	rs119103266
ensembl	rs119103266
geneview	rs119103266
scholar	rs119103266
google	rs119103266
pharmgkb	rs119103266
gwascentral	rs119103266
openSNP	rs119103266
23andMe	rs119103266
SNPshot	rs119103266
SNPdbe	rs119103266
MSV3d	rs119103266
GWAS Ctlg	rs119103266

Max Magnitude

0

OMIM	608507
Desc
Variant	0012
Related	also

ClinVar
Risk	rs119103266(T;T)
Alt	rs119103266(T;T)
Reference	Rs119103266(C;C)
Significance	Pathogenic
Disease	Hereditary motor and sensory neuropathy with optic atrophy
Variation	info
Gene	MFN2
CLNDBN	Hereditary motor and sensory neuropathy with optic atrophy
Reversed	0
HGVS	NC_000001.10:g.12058844C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002368.5,