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rs63750331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750331(A;A)
Make rs63750331(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position44349167
GeneGRN
is asnp
is mentioned by
dbSNPrs63750331
ebirs63750331
HLIrs63750331
Exacrs63750331
Varsomers63750331
Maprs63750331
PheGenIrs63750331
hapmaprs63750331
1000 genomesrs63750331
hgdprs63750331
ensemblrs63750331
gopubmedrs63750331
geneviewrs63750331
scholarrs63750331
googlers63750331
pharmgkbrs63750331
gwascentralrs63750331
openSNPrs63750331
23andMers63750331
23andMe allrs63750331
SNP Nexus

SNPshotrs63750331
SNPdbers63750331
MSV3drs63750331
GWAS Ctlgrs63750331
Max Magnitude0
OMIM138945
Desc
Variant0004
Relatedalso


ClinVar
Risk rs63750331(A;A)
Alt rs63750331(A;A)
Reference rs63750331(G;G)
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.42426535G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017382.28, RCV000084420.1,