rs1057517987

Orientation

plus

Stabilized

plus

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

Make rs1057517987(C;T)

Make rs1057517987(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

12004083

Gene

MFN2

is a	snp
is	mentioned by
dbSNP	rs1057517987
dbSNP (classic)	rs1057517987
ClinGen	rs1057517987
ebi	rs1057517987
HLI	rs1057517987
Exac	rs1057517987
Gnomad	rs1057517987
Varsome	rs1057517987
LitVar	rs1057517987
Map	rs1057517987
PheGenI	rs1057517987
Biobank	rs1057517987
1000 genomes	rs1057517987
hgdp	rs1057517987
ensembl	rs1057517987
geneview	rs1057517987
scholar	rs1057517987
google	rs1057517987
pharmgkb	rs1057517987
gwascentral	rs1057517987
openSNP	rs1057517987
23andMe	rs1057517987
SNPshot	rs1057517987
SNPdbe	rs1057517987
MSV3d	rs1057517987
GWAS Ctlg	rs1057517987

Max Magnitude

0

ClinVar
Risk	rs1057517987(T;T)
Alt	rs1057517987(T;T)
Reference	Rs1057517987(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MFN2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.12064140C>T
CLNSRC
CLNACC	RCV000413487.1,