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rs398123158

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123158(A;G)
Make rs398123158(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154380880
GeneEMD
is asnp
is mentioned by
dbSNPrs398123158
ebirs398123158
HLIrs398123158
Exacrs398123158
Varsomers398123158
Maprs398123158
PheGenIrs398123158
hapmaprs398123158
1000 genomesrs398123158
hgdprs398123158
ensemblrs398123158
gopubmedrs398123158
geneviewrs398123158
scholarrs398123158
googlers398123158
pharmgkbrs398123158
gwascentralrs398123158
openSNPrs398123158
23andMers398123158
23andMe allrs398123158
SNP Nexus

SNPshotrs398123158
SNPdbers398123158
MSV3drs398123158
GWAS Ctlgrs398123158
Max Magnitude0
ClinVar
Risk rs398123158(G;G)
Alt rs398123158(G;G)
Reference rs398123158(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene EMD
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153609240A>G
CLNSRC ClinVar
CLNACC RCV000078132.4,