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rs398123241

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123241(A;A)
Make rs398123241(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position134498389
GeneHPRT1
is asnp
is mentioned by
dbSNPrs398123241
ebirs398123241
HLIrs398123241
Exacrs398123241
Varsomers398123241
Maprs398123241
PheGenIrs398123241
hapmaprs398123241
1000 genomesrs398123241
hgdprs398123241
ensemblrs398123241
gopubmedrs398123241
geneviewrs398123241
scholarrs398123241
googlers398123241
pharmgkbrs398123241
gwascentralrs398123241
openSNPrs398123241
23andMers398123241
23andMe allrs398123241
SNP Nexus

SNPshotrs398123241
SNPdbers398123241
MSV3drs398123241
GWAS Ctlgrs398123241
Max Magnitude0
ClinVar
Risk rs398123241(A;A)
Alt rs398123241(A;A)
Reference rs398123241(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene HPRT1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.133632419G>A
CLNSRC HGMD
CLNACC RCV000078345.4,