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rs398123283

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123283(C;T)
Make rs398123283(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position43958537
GeneNDP
is asnp
is mentioned by
dbSNPrs398123283
ebirs398123283
HLIrs398123283
Exacrs398123283
Varsomers398123283
Maprs398123283
PheGenIrs398123283
hapmaprs398123283
1000 genomesrs398123283
hgdprs398123283
ensemblrs398123283
gopubmedrs398123283
geneviewrs398123283
scholarrs398123283
googlers398123283
pharmgkbrs398123283
gwascentralrs398123283
openSNPrs398123283
23andMers398123283
23andMe allrs398123283
SNP Nexus

SNPshotrs398123283
SNPdbers398123283
MSV3drs398123283
GWAS Ctlgrs398123283
Max Magnitude0
ClinVar
Risk rs398123283(T;T)
Alt rs398123283(T;T)
Reference rs398123283(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NDP
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.43817783G>A
CLNSRC HGMD
CLNACC RCV000078465.4,