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rs398124396

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs398124396(-;-)
Make rs398124396(-;AT)
ReferenceGRCh38 38.1/141
Chromosome12
Position101770482
GeneGNPTAB
is asnp
is mentioned by
dbSNPrs398124396
ebirs398124396
HLIrs398124396
Exacrs398124396
Varsomers398124396
Maprs398124396
PheGenIrs398124396
hapmaprs398124396
1000 genomesrs398124396
hgdprs398124396
ensemblrs398124396
gopubmedrs398124396
geneviewrs398124396
scholarrs398124396
googlers398124396
pharmgkbrs398124396
gwascentralrs398124396
openSNPrs398124396
23andMers398124396
23andMe allrs398124396
SNP Nexus

SNPshotrs398124396
SNPdbers398124396
MSV3drs398124396
GWAS Ctlgrs398124396
Max Magnitude0
ClinVar
Risk rs398124396(;)
Alt rs398124396(;)
Reference rs398124396(AT;AT)
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.102164260_102164261delAT
CLNSRC ClinVar
CLNACC RCV000082185.3, RCV000180685.1,