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rs781689303

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs781689303(-;-)
Make rs781689303(-;TC)
Make rs781689303(TC;TC)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position101753413
GeneGNPTAB
is asnp
is mentioned by
dbSNPrs781689303
dbSNP (old)rs781689303
ClinGenrs781689303
ebirs781689303
HLIrs781689303
Exacrs781689303
Gnomadrs781689303
Varsomers781689303
Maprs781689303
PheGenIrs781689303
Biobankrs781689303
1000 genomesrs781689303
hgdprs781689303
ensemblrs781689303
gopubmedrs781689303
geneviewrs781689303
scholarrs781689303
googlers781689303
pharmgkbrs781689303
gwascentralrs781689303
openSNPrs781689303
23andMers781689303
23andMe allrs781689303
SNP Nexus

SNPshotrs781689303
SNPdbers781689303
MSV3drs781689303
GWAS Ctlgrs781689303
Max Magnitude0
ClinVar
Risk rs781689303(-;-)
Alt rs781689303(-;-)
Reference Rs781689303(CT;CT)
Significance Pathogenic
Disease I cell disease
Variation info
Gene GNPTAB
CLNDBN I cell disease
Reversed 0
HGVS NC_000012.11:g.102147191_102147192delCT
CLNSRC
CLNACC RCV000175480.1,