Rs104894756

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Orientationplus
is asnp
is mentioned by
dbSNPrs104894756
PheGenIrs104894756
nextbiors104894756
hapmaprs104894756
1000 genomesrs104894756
hgdprs104894756
ensemblrs104894756
gopubmedrs104894756
geneviewrs104894756
scholarrs104894756
googlers104894756
pharmgkbrs104894756
gwascentralrs104894756
openSNPrs104894756
23andMers104894756
23andMe allrs104894756
SNP Nexus

SNPshotrs104894756
SNPdbers104894756
MSV3drs104894756
GeneAVPR2
ChromosomeX
Orientationplus
Position153171370
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894756(A;A)
Make rs104894756(A;G)
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 5
Disease Nephrogenic diabetes insipidus, Nephrogenic syndrome of inappropriate antidiuresis
ClinVar info
Gene AVPR2
CLNDBN Nephrogenic diabetes insipidus, X-linked, Nephrogenic syndrome of inappropriate antidiuresis
Reversed 0
CLNHGVS NC_000023.10:g.153171370G>A; NC_000023.10:g.153171370G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011596.6, RCV000011602.2