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rs63750077

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750077(C;T)
Make rs63750077(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position44350251
GeneGRN
is asnp
is mentioned by
dbSNPrs63750077
ebirs63750077
HLIrs63750077
Exacrs63750077
Varsomers63750077
Maprs63750077
PheGenIrs63750077
hapmaprs63750077
1000 genomesrs63750077
hgdprs63750077
ensemblrs63750077
gopubmedrs63750077
geneviewrs63750077
scholarrs63750077
googlers63750077
pharmgkbrs63750077
gwascentralrs63750077
openSNPrs63750077
23andMers63750077
23andMe allrs63750077
SNP Nexus

SNPshotrs63750077
SNPdbers63750077
MSV3drs63750077
GWAS Ctlgrs63750077
Max Magnitude0
OMIM138945
Desc
Variant0002
Relatedalso


ClinVar
Risk rs63750077(T;T)
Alt rs63750077(T;T)
Reference rs63750077(C;C)
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.42427619C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017380.27, RCV000084439.1,