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rs193922123

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922123(A;A)
Make rs193922123(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153906575
GeneAVPR2
is asnp
is mentioned by
dbSNPrs193922123
ebirs193922123
HLIrs193922123
Exacrs193922123
Varsomers193922123
Maprs193922123
PheGenIrs193922123
hapmaprs193922123
1000 genomesrs193922123
hgdprs193922123
ensemblrs193922123
gopubmedrs193922123
geneviewrs193922123
scholarrs193922123
googlers193922123
pharmgkbrs193922123
gwascentralrs193922123
openSNPrs193922123
23andMers193922123
23andMe allrs193922123
SNP Nexus

SNPshotrs193922123
SNPdbers193922123
MSV3drs193922123
GWAS Ctlgrs193922123
Max Magnitude0
ClinVar
Risk rs193922123(A;A)
Alt rs193922123(A;A)
Reference rs193922123(C;C)
Significance Probable-Pathogenic
Disease Nephrogenic diabetes insipidus
Variation info
Gene AVPR2
CLNDBN Nephrogenic diabetes insipidus
Reversed 0
HGVS NC_000023.10:g.153172029C>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029400.1,