rs775332895

Orientation

plus

Stabilized

plus

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

Make rs775332895(A;A)

Make rs775332895(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

23767396

Gene	CHCHD10, LOC107985577

is a	snp
is	mentioned by
dbSNP	rs775332895
dbSNP (classic)	rs775332895
ClinGen	rs775332895
ebi	rs775332895
HLI	rs775332895
Exac	rs775332895
Gnomad	rs775332895
Varsome	rs775332895
LitVar	rs775332895
Map	rs775332895
PheGenI	rs775332895
Biobank	rs775332895
1000 genomes	rs775332895
hgdp	rs775332895
ensembl	rs775332895
geneview	rs775332895
scholar	rs775332895
google	rs775332895
pharmgkb	rs775332895
gwascentral	rs775332895
openSNP	rs775332895
23andMe	rs775332895
SNPshot	rs775332895
SNPdbe	rs775332895
MSV3d	rs775332895
GWAS Ctlg	rs775332895

Max Magnitude

0

ClinVar
Risk	rs775332895(A;A)
Alt	rs775332895(A;A)
Reference	Rs775332895(G;G)
Significance	Pathogenic
Disease	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2
Variation	info
Gene	CHCHD10
CLNDBN	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2
Reversed	0
HGVS	NC_000022.10:g.24109583G>A
CLNSRC
CLNACC	RCV000192233.1,