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rs121964889

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964889(G;T)
Make rs121964889(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position3082788
GeneAVP
is asnp
is mentioned by
dbSNPrs121964889
ebirs121964889
HLIrs121964889
Exacrs121964889
Varsomers121964889
Maprs121964889
PheGenIrs121964889
hapmaprs121964889
1000 genomesrs121964889
hgdprs121964889
ensemblrs121964889
gopubmedrs121964889
geneviewrs121964889
scholarrs121964889
googlers121964889
pharmgkbrs121964889
gwascentralrs121964889
openSNPrs121964889
23andMers121964889
23andMe allrs121964889
SNP Nexus

SNPshotrs121964889
SNPdbers121964889
MSV3drs121964889
GWAS Ctlgrs121964889
Max Magnitude0
OMIM192340
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121964889(A,T;A,T)
Alt rs121964889(A,T;A,T)
Reference rs121964889(G;G)
Significance Pathogenic
Disease Neurohypophyseal diabetes insipidus
Variation info
Gene AVP
CLNDBN Neurohypophyseal diabetes insipidus
Reversed 1
HGVS NC_000020.10:g.3063434C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012999.22,