rs879253939

Orientation

plus

Stabilized

plus

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

Make rs879253939(C;T)

Make rs879253939(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

12004029

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs879253939
dbSNP (classic)	rs879253939
ClinGen	rs879253939
ebi	rs879253939
HLI	rs879253939
Exac	rs879253939
Gnomad	rs879253939
Varsome	rs879253939
LitVar	rs879253939
Map	rs879253939
PheGenI	rs879253939
Biobank	rs879253939
1000 genomes	rs879253939
hgdp	rs879253939
ensembl	rs879253939
geneview	rs879253939
scholar	rs879253939
google	rs879253939
pharmgkb	rs879253939
gwascentral	rs879253939
openSNP	rs879253939
23andMe	rs879253939
SNPshot	rs879253939
SNPdbe	rs879253939
MSV3d	rs879253939
GWAS Ctlg	rs879253939

Max Magnitude

0

ClinVar
Risk	rs879253939(T;T)
Alt	rs879253939(T;T)
Reference	Rs879253939(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MFN2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.12064086C>T
CLNSRC
CLNACC	RCV000235812.1,