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rs775332895

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775332895(A;A)
Make rs775332895(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position23767396
GeneCHCHD10
is asnp
is mentioned by
dbSNPrs775332895
ebirs775332895
HLIrs775332895
Exacrs775332895
Varsomers775332895
Maprs775332895
PheGenIrs775332895
hapmaprs775332895
1000 genomesrs775332895
hgdprs775332895
ensemblrs775332895
gopubmedrs775332895
geneviewrs775332895
scholarrs775332895
googlers775332895
pharmgkbrs775332895
gwascentralrs775332895
openSNPrs775332895
23andMers775332895
23andMe allrs775332895
SNP Nexus

SNPshotrs775332895
SNPdbers775332895
MSV3drs775332895
GWAS Ctlgrs775332895
Max Magnitude0
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,