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rs397507448

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507448(-;-)
Make rs397507448(-;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position101768046
GeneGNPTAB
is asnp
is mentioned by
dbSNPrs397507448
ebirs397507448
HLIrs397507448
Exacrs397507448
Varsomers397507448
Maprs397507448
PheGenIrs397507448
hapmaprs397507448
1000 genomesrs397507448
hgdprs397507448
ensemblrs397507448
gopubmedrs397507448
geneviewrs397507448
scholarrs397507448
googlers397507448
pharmgkbrs397507448
gwascentralrs397507448
openSNPrs397507448
23andMers397507448
23andMe allrs397507448
SNP Nexus

SNPshotrs397507448
SNPdbers397507448
MSV3drs397507448
GWAS Ctlgrs397507448
Max Magnitude0
ClinVar
Risk rs397507448(;)
Alt rs397507448(;)
Reference rs397507448(G;G)
Significance Pathogenic
Disease I cell disease
Variation info
Gene GNPTAB
CLNDBN I cell disease
Reversed 1
HGVS NC_000012.11:g.102161824delC
CLNSRC ClinVar GeneReviews
CLNACC RCV000032299.1,