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rs63751165

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751165(A;A)
Make rs63751165(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position46010401
GeneMAPT
is asnp
is mentioned by
dbSNPrs63751165
ebirs63751165
HLIrs63751165
Exacrs63751165
Varsomers63751165
Maprs63751165
PheGenIrs63751165
hapmaprs63751165
1000 genomesrs63751165
hgdprs63751165
ensemblrs63751165
gopubmedrs63751165
geneviewrs63751165
scholarrs63751165
googlers63751165
pharmgkbrs63751165
gwascentralrs63751165
openSNPrs63751165
23andMers63751165
23andMe allrs63751165
SNP Nexus

SNPshotrs63751165
SNPdbers63751165
MSV3drs63751165
GWAS Ctlgrs63751165
Max Magnitude0
OMIM157140
Desc
Variant0010
Relatedalso


ClinVar
Risk rs63751165(A;A)
Alt rs63751165(A;A)
Reference rs63751165(G;G)
Significance Pathogenic
Disease Frontotemporal dementia not provided
Variation info
Gene MAPT
CLNDBN Frontotemporal dementia not provided
Reversed 0
HGVS NC_000017.10:g.44087767G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015323.26, RCV000084530.1,