Rs104894751

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Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894751(A;A)
Make rs104894751(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153905719
GeneAVPR2
is asnp
is mentioned by
dbSNPrs104894751
Exacrs104894751
PheGenIrs104894751
nextbiors104894751
hapmaprs104894751
1000 genomesrs104894751
hgdprs104894751
ensemblrs104894751
gopubmedrs104894751
geneviewrs104894751
scholarrs104894751
googlers104894751
pharmgkbrs104894751
gwascentralrs104894751
openSNPrs104894751
23andMers104894751
23andMe allrs104894751
SNP Nexus

SNPshotrs104894751
SNPdbers104894751
MSV3drs104894751
OMIM300538
Desc
Variant0008
Relatedalso
ClinVar
Risk rs104894751(A;A)
Alt rs104894751(A;A)
Reference rs104894751(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.153171173G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011589.8,