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rs398124399

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ACAG;ACAG) 0 common in clinvar
Make rs398124399(-;-)
Make rs398124399(-;ACAG)
ReferenceGRCh38 38.1/141
Chromosome12
Position101780574
GeneGNPTAB
is asnp
is mentioned by
dbSNPrs398124399
ebirs398124399
HLIrs398124399
Exacrs398124399
Varsomers398124399
Maprs398124399
PheGenIrs398124399
hapmaprs398124399
1000 genomesrs398124399
hgdprs398124399
ensemblrs398124399
gopubmedrs398124399
geneviewrs398124399
scholarrs398124399
googlers398124399
pharmgkbrs398124399
gwascentralrs398124399
openSNPrs398124399
23andMers398124399
23andMe allrs398124399
SNP Nexus

SNPshotrs398124399
SNPdbers398124399
MSV3drs398124399
GWAS Ctlgrs398124399
Max Magnitude0
ClinVar
Risk rs398124399(;)
Alt rs398124399(;)
Reference rs398124399(ACAG;ACAG)
Significance Pathogenic
Disease I cell disease not provided
Variation info
Gene GNPTAB
CLNDBN I cell disease not provided
Reversed 1
HGVS NC_000012.11:g.102174352_102174355delCTGT
CLNSRC HGMD
CLNACC RCV000031989.3, RCV000082195.3,