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rs63751006

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751006(C;C)
Make rs63751006(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position44349166
GeneGRN
is asnp
is mentioned by
dbSNPrs63751006
ebirs63751006
HLIrs63751006
Exacrs63751006
Varsomers63751006
Maprs63751006
PheGenIrs63751006
hapmaprs63751006
1000 genomesrs63751006
hgdprs63751006
ensemblrs63751006
gopubmedrs63751006
geneviewrs63751006
scholarrs63751006
googlers63751006
pharmgkbrs63751006
gwascentralrs63751006
openSNPrs63751006
23andMers63751006
23andMe allrs63751006
SNP Nexus

SNPshotrs63751006
SNPdbers63751006
MSV3drs63751006
GWAS Ctlgrs63751006
Max Magnitude0
OMIM138945
Desc
Variant0003
Relatedalso


ClinVar
Risk rs63751006(C;C)
Alt rs63751006(C;C)
Reference Rs63751006(T;T)
Significance Pathogenic
Disease Frontotemporal dementia not provided
Variation info
Gene GRN
CLNDBN Frontotemporal dementia, ubiquitin-positive not provided
Reversed 0
HGVS NC_000017.10:g.42426534T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017381.27, RCV000084419.1,