Rs104894748

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Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894748(G;T)
Make rs104894748(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153906059
GeneAVPR2
is asnp
is mentioned by
dbSNPrs104894748
Exacrs104894748
PheGenIrs104894748
nextbiors104894748
hapmaprs104894748
1000 genomesrs104894748
hgdprs104894748
ensemblrs104894748
gopubmedrs104894748
geneviewrs104894748
scholarrs104894748
googlers104894748
pharmgkbrs104894748
gwascentralrs104894748
openSNPrs104894748
23andMers104894748
23andMe allrs104894748
SNP Nexus

SNPshotrs104894748
SNPdbers104894748
MSV3drs104894748
Max Magnitude0
OMIM300538
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894748(T;T)
Alt rs104894748(T;T)
Reference rs104894748(G;G)
Significance Pathogenic
Disease Nephrogenic diabetes insipidus
Variation info
Gene AVPR2
CLNDBN Nephrogenic diabetes insipidus, X-linked
Reversed 0
HGVS NC_000023.10:g.153171513G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011584.1,