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rs747789493

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs747789493(-;T)
Make rs747789493(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position101765010
GeneGNPTAB
is asnp
is mentioned by
dbSNPrs747789493
dbSNP (old)rs747789493
ClinGenrs747789493
ebirs747789493
HLIrs747789493
Exacrs747789493
Gnomadrs747789493
Varsomers747789493
Maprs747789493
PheGenIrs747789493
Biobankrs747789493
1000 genomesrs747789493
hgdprs747789493
ensemblrs747789493
gopubmedrs747789493
geneviewrs747789493
scholarrs747789493
googlers747789493
pharmgkbrs747789493
gwascentralrs747789493
openSNPrs747789493
23andMers747789493
23andMe allrs747789493
SNP Nexus

SNPshotrs747789493
SNPdbers747789493
MSV3drs747789493
GWAS Ctlgrs747789493
Max Magnitude0
ClinVar
Risk rs747789493(T;T)
Alt rs747789493(T;T)
Reference Rs747789493(-;-)
Significance Pathogenic
Disease I cell disease
Variation info
Gene GNPTAB
CLNDBN I cell disease
Reversed 0
HGVS NC_000012.11:g.102158789dupT
CLNSRC
CLNACC RCV000174596.1,