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rs104894417

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894417(A;A)
Make rs104894417(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position48261222
GeneFITM1, ITM2B
is asnp
is mentioned by
dbSNPrs104894417
ebirs104894417
HLIrs104894417
Exacrs104894417
Varsomers104894417
Maprs104894417
PheGenIrs104894417
hapmaprs104894417
1000 genomesrs104894417
hgdprs104894417
ensemblrs104894417
gopubmedrs104894417
geneviewrs104894417
scholarrs104894417
googlers104894417
pharmgkbrs104894417
gwascentralrs104894417
openSNPrs104894417
23andMers104894417
23andMe allrs104894417
SNP Nexus

SNPshotrs104894417
SNPdbers104894417
MSV3drs104894417
GWAS Ctlgrs104894417
Max Magnitude0
OMIM603904
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894417(A;A)
Alt rs104894417(A;A)
Reference rs104894417(T;T)
Significance Pathogenic
Disease Dementia familial British
Variation info
Gene ITM2B
CLNDBN Dementia familial British
Reversed 0
HGVS NC_000013.10:g.48835358T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006345.3,