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rs587777912

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777912(-;-)
Make rs587777912(-;T)
Make rs587777912(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position101761344
GeneGNPTAB
is asnp
is mentioned by
dbSNPrs587777912
ebirs587777912
HLIrs587777912
Exacrs587777912
Varsomers587777912
Maprs587777912
PheGenIrs587777912
hapmaprs587777912
1000 genomesrs587777912
hgdprs587777912
ensemblrs587777912
gopubmedrs587777912
geneviewrs587777912
scholarrs587777912
googlers587777912
pharmgkbrs587777912
gwascentralrs587777912
openSNPrs587777912
23andMers587777912
23andMe allrs587777912
SNP Nexus

SNPshotrs587777912
SNPdbers587777912
MSV3drs587777912
GWAS Ctlgrs587777912
Max Magnitude0
ClinVar
Risk rs587777912(T;T)
Alt rs587777912(T;T)
Reference rs587777912(;)
Significance Pathogenic
Disease I cell disease
Variation info
Gene GNPTAB
CLNDBN I cell disease
Reversed 1
HGVS NC_000012.11:g.102155123dupA
CLNSRC
CLNACC RCV000031977.2,