Have questions? Visit https://www.reddit.com/r/SNPedia

rs121964882

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964882(A;A)
Make rs121964882(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position3083037
GeneAVP
is asnp
is mentioned by
dbSNPrs121964882
ClinGenrs121964882
ebirs121964882
HLIrs121964882
Exacrs121964882
Varsomers121964882
Maprs121964882
PheGenIrs121964882
hapmaprs121964882
1000 genomesrs121964882
hgdprs121964882
ensemblrs121964882
gopubmedrs121964882
geneviewrs121964882
scholarrs121964882
googlers121964882
pharmgkbrs121964882
gwascentralrs121964882
openSNPrs121964882
23andMers121964882
23andMe allrs121964882
SNP Nexus

SNPshotrs121964882
SNPdbers121964882
MSV3drs121964882
GWAS Ctlgrs121964882
Max Magnitude0
OMIM192340
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121964882(A;A)
Alt rs121964882(A;A)
Reference Rs121964882(G;G)
Significance Pathogenic
Disease Neurohypophyseal diabetes insipidus
Variation info
Gene AVP
CLNDBN Neurohypophyseal diabetes insipidus
Reversed 1
HGVS NC_000020.10:g.3063683C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000012988.24,