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rs551521196

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs551521196(A;A)
Make rs551521196(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position23767535
GeneCHCHD10
is asnp
is mentioned by
dbSNPrs551521196
ebirs551521196
HLIrs551521196
Exacrs551521196
Varsomers551521196
Maprs551521196
PheGenIrs551521196
hapmaprs551521196
1000 genomesrs551521196
hgdprs551521196
ensemblrs551521196
gopubmedrs551521196
geneviewrs551521196
scholarrs551521196
googlers551521196
pharmgkbrs551521196
gwascentralrs551521196
openSNPrs551521196
23andMers551521196
23andMe allrs551521196
SNP Nexus

SNPshotrs551521196
SNPdbers551521196
MSV3drs551521196
GWAS Ctlgrs551521196
Max Magnitude0
ClinVar
Risk rs551521196(A;A)
Alt rs551521196(A;A)
Reference rs551521196(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.24109722G>A
CLNSRC
CLNACC RCV000192231.1,