rs587777574

Orientation

plus

Stabilized

minus

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

Make rs587777574(A;A)

Make rs587777574(A;G)

Reference

GRCh38 38.1/142

Chromosome

22

Position

23767459

Gene	CHCHD10, LOC107985577

is a	snp
is	mentioned by
dbSNP	rs587777574
dbSNP (classic)	rs587777574
ClinGen	rs587777574
ebi	rs587777574
HLI	rs587777574
Exac	rs587777574
Gnomad	rs587777574
Varsome	rs587777574
LitVar	rs587777574
Map	rs587777574
PheGenI	rs587777574
Biobank	rs587777574
1000 genomes	rs587777574
hgdp	rs587777574
ensembl	rs587777574
geneview	rs587777574
scholar	rs587777574
google	rs587777574
pharmgkb	rs587777574
gwascentral	rs587777574
openSNP	rs587777574
23andMe	rs587777574
SNPshot	rs587777574
SNPdbe	rs587777574
MSV3d	rs587777574
GWAS Ctlg	rs587777574

Max Magnitude

0

ClinVar
Risk	rs587777574(A;A) Rs587777574(G;G)
Alt	rs587777574(A;A) Rs587777574(G;G)
Reference	Rs587777574(C;C)
Significance	Pathogenic
Disease	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Myopathy
Variation	info
Gene	CHCHD10
CLNDBN	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Myopathy, isolated mitochondrial, autosomal dominant
Reversed	1
HGVS	NC_000022.10:g.24109646G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000128857.5, RCV000192232.1,