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rs63749801

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGTC;AGTC) 0 common in clinvar
(I;I) 0
Make rs63749801(-;-)
Make rs63749801(-;CAGT)
Make rs63749801(CAGT;CAGT)
ReferenceGRCh38 38.1/142
Chromosome17
Position44350266
GeneGRN
is asnp
is mentioned by
dbSNPrs63749801
ebirs63749801
HLIrs63749801
Exacrs63749801
Varsomers63749801
Maprs63749801
PheGenIrs63749801
hapmaprs63749801
1000 genomesrs63749801
hgdprs63749801
ensemblrs63749801
gopubmedrs63749801
geneviewrs63749801
scholarrs63749801
googlers63749801
pharmgkbrs63749801
gwascentralrs63749801
openSNPrs63749801
23andMers63749801
23andMe allrs63749801
SNP Nexus

SNPshotrs63749801
SNPdbers63749801
MSV3drs63749801
GWAS Ctlgrs63749801
Max Magnitude0


ClinVar
Risk rs63749801(;)
Alt rs63749801(;)
Reference rs63749801(AGTC;AGTC)
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.42427634_42427637delCAGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000017384.28, RCV000084442.1,