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rs193922119

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922119(-;-)
Make rs193922119(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153906276
GeneAVPR2
is asnp
is mentioned by
dbSNPrs193922119
ebirs193922119
HLIrs193922119
Exacrs193922119
Varsomers193922119
Maprs193922119
PheGenIrs193922119
hapmaprs193922119
1000 genomesrs193922119
hgdprs193922119
ensemblrs193922119
gopubmedrs193922119
geneviewrs193922119
scholarrs193922119
googlers193922119
pharmgkbrs193922119
gwascentralrs193922119
openSNPrs193922119
23andMers193922119
23andMe allrs193922119
SNP Nexus

SNPshotrs193922119
SNPdbers193922119
MSV3drs193922119
GWAS Ctlgrs193922119
Max Magnitude0
ClinVar
Risk rs193922119(;)
Alt rs193922119(;)
Reference rs193922119(G;G)
Significance Probable-Pathogenic
Disease Nephrogenic diabetes insipidus
Variation info
Gene AVPR2
CLNDBN Nephrogenic diabetes insipidus
Reversed 0
HGVS NC_000023.10:g.153171730delG
CLNSRC ClinVar LabCorp
CLNACC RCV000029396.1,