Rs104894756

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Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894756(A;A)
Make rs104894756(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153905916
GeneAVPR2
is asnp
is mentioned by
dbSNPrs104894756
Exacrs104894756
PheGenIrs104894756
nextbiors104894756
hapmaprs104894756
1000 genomesrs104894756
hgdprs104894756
ensemblrs104894756
gopubmedrs104894756
geneviewrs104894756
scholarrs104894756
googlers104894756
pharmgkbrs104894756
gwascentralrs104894756
openSNPrs104894756
23andMers104894756
23andMe allrs104894756
SNP Nexus

SNPshotrs104894756
SNPdbers104894756
MSV3drs104894756
OMIM300538
Desc
Variant0015
Relatedalso
OMIM300538
Desc
Variant0022
Relatedalso
ClinVar
Risk rs104894756(A,T;A,T)
Alt rs104894756(A,T;A,T)
Reference rs104894756(G;G)
Significance Pathogenic
Disease Nephrogenic diabetes insipidus Nephrogenic syndrome of inappropriate antidiuresis
Variation info
Gene AVPR2
CLNDBN Nephrogenic diabetes insipidus, X-linked Nephrogenic syndrome of inappropriate antidiuresis
Reversed 0
HGVS NC_000023.10:g.153171370G>A; NC_000023.10:g.153171370G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011596.6, RCV000011602.2,