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rs398124398

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124398(-;-)
Make rs398124398(-;A)
ReferenceGRCh38 38.1/141
Chromosome12
Position101761583
GeneGNPTAB
is asnp
is mentioned by
dbSNPrs398124398
ebirs398124398
HLIrs398124398
Exacrs398124398
Varsomers398124398
Maprs398124398
PheGenIrs398124398
hapmaprs398124398
1000 genomesrs398124398
hgdprs398124398
ensemblrs398124398
gopubmedrs398124398
geneviewrs398124398
scholarrs398124398
googlers398124398
pharmgkbrs398124398
gwascentralrs398124398
openSNPrs398124398
23andMers398124398
23andMe allrs398124398
SNP Nexus

SNPshotrs398124398
SNPdbers398124398
MSV3drs398124398
GWAS Ctlgrs398124398
Max Magnitude0
ClinVar
Risk rs398124398(;)
Alt rs398124398(;)
Reference rs398124398(A;A)
Significance Pathogenic
Disease not provided I cell disease
Variation info
Gene GNPTAB
CLNDBN not provided I cell disease
Reversed 1
HGVS NC_000012.11:g.102155361delT
CLNSRC ClinVar
CLNACC RCV000082190.3, RCV000174796.1,