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rs397515326

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515326(A;T)
Make rs397515326(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position26193346
GeneHNRNPA2B1
is asnp
is mentioned by
dbSNPrs397515326
ebirs397515326
HLIrs397515326
Exacrs397515326
Varsomers397515326
Maprs397515326
PheGenIrs397515326
hapmaprs397515326
1000 genomesrs397515326
hgdprs397515326
ensemblrs397515326
gopubmedrs397515326
geneviewrs397515326
scholarrs397515326
googlers397515326
pharmgkbrs397515326
gwascentralrs397515326
openSNPrs397515326
23andMers397515326
23andMe allrs397515326
SNP Nexus

SNPshotrs397515326
SNPdbers397515326
MSV3drs397515326
GWAS Ctlgrs397515326
Max Magnitude0
ClinVar
Risk rs397515326(T;T)
Alt rs397515326(T;T)
Reference rs397515326(A;A)
Significance Pathogenic
Disease Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2
Variation info
Gene HNRNPA2B1
CLNDBN Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2
Reversed 1
HGVS NC_000007.13:g.26232966T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000055652.8,