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rs63749817

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63749817(A;A)
Make rs63749817(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44350801
GeneGRN
is asnp
is mentioned by
dbSNPrs63749817
ebirs63749817
HLIrs63749817
Exacrs63749817
Varsomers63749817
Maprs63749817
PheGenIrs63749817
hapmaprs63749817
1000 genomesrs63749817
hgdprs63749817
ensemblrs63749817
gopubmedrs63749817
geneviewrs63749817
scholarrs63749817
googlers63749817
pharmgkbrs63749817
gwascentralrs63749817
openSNPrs63749817
23andMers63749817
23andMe allrs63749817
SNP Nexus

SNPshotrs63749817
SNPdbers63749817
MSV3drs63749817
GWAS Ctlgrs63749817
Max Magnitude0
ClinVar
Risk rs63749817(A,C;A,C)
Alt rs63749817(A,C;A,C)
Reference rs63749817(G;G)
Significance Pathogenic
Disease Frontotemporal dementia not provided
Variation info
Gene GRN
CLNDBN Frontotemporal dementia not provided
Reversed 0
HGVS NC_000017.10:g.42428169G>A; NC_000017.10:g.42428169G>C
CLNSRC
CLNACC RCV000185615.1, RCV000084452.1,