Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507562

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507562(C;C)
Make rs397507562(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position101757311
GeneGNPTAB
is asnp
is mentioned by
dbSNPrs397507562
ebirs397507562
HLIrs397507562
Exacrs397507562
Varsomers397507562
Maprs397507562
PheGenIrs397507562
hapmaprs397507562
1000 genomesrs397507562
hgdprs397507562
ensemblrs397507562
gopubmedrs397507562
geneviewrs397507562
scholarrs397507562
googlers397507562
pharmgkbrs397507562
gwascentralrs397507562
openSNPrs397507562
23andMers397507562
23andMe allrs397507562
SNP Nexus

SNPshotrs397507562
SNPdbers397507562
MSV3drs397507562
GWAS Ctlgrs397507562
Max Magnitude0
ClinVar
Risk rs397507562(C;C)
Alt rs397507562(C;C)
Reference rs397507562(G;G)
Significance Pathogenic
Disease I cell disease
Variation info
Gene GNPTAB
CLNDBN I cell disease
Reversed 1
HGVS NC_000012.11:g.102151089C>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000034158.2,