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rs121964886

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964886(G;T)
Make rs121964886(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position3083012
GeneAVP
is asnp
is mentioned by
dbSNPrs121964886
ebirs121964886
HLIrs121964886
Exacrs121964886
Varsomers121964886
Maprs121964886
PheGenIrs121964886
hapmaprs121964886
1000 genomesrs121964886
hgdprs121964886
ensemblrs121964886
gopubmedrs121964886
geneviewrs121964886
scholarrs121964886
googlers121964886
pharmgkbrs121964886
gwascentralrs121964886
openSNPrs121964886
23andMers121964886
23andMe allrs121964886
SNP Nexus

SNPshotrs121964886
SNPdbers121964886
MSV3drs121964886
GWAS Ctlgrs121964886
Max Magnitude0
OMIM192340
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121964886(T;T)
Alt rs121964886(T;T)
Reference rs121964886(G;G)
Significance Pathogenic
Disease Neurohypophyseal diabetes insipidus
Variation info
Gene AVP
CLNDBN Neurohypophyseal diabetes insipidus
Reversed 1
HGVS NC_000020.10:g.3063658C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012995.22,