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rs398123155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123155(-;-)
Make rs398123155(-;T)
Make rs398123155(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154379993
GeneEMD
is asnp
is mentioned by
dbSNPrs398123155
ebirs398123155
HLIrs398123155
Exacrs398123155
Varsomers398123155
Maprs398123155
PheGenIrs398123155
hapmaprs398123155
1000 genomesrs398123155
hgdprs398123155
ensemblrs398123155
gopubmedrs398123155
geneviewrs398123155
scholarrs398123155
googlers398123155
pharmgkbrs398123155
gwascentralrs398123155
openSNPrs398123155
23andMers398123155
23andMe allrs398123155
SNP Nexus

SNPshotrs398123155
SNPdbers398123155
MSV3drs398123155
GWAS Ctlgrs398123155
Max Magnitude0
ClinVar
Risk rs398123155(T;T)
Alt rs398123155(T;T)
Reference rs398123155(;)
Significance Pathogenic
Disease not provided
Variation info
Gene EMD
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153608353_153608354insT
CLNSRC ClinVar
CLNACC RCV000078129.4,