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

rs104894331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894331(A;G)
Make rs104894331(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position49951033
GeneAQP2, LOC101927318
is asnp
is mentioned by
dbSNPrs104894331
ebirs104894331
HLIrs104894331
Exacrs104894331
Varsomers104894331
Maprs104894331
PheGenIrs104894331
hapmaprs104894331
1000 genomesrs104894331
hgdprs104894331
ensemblrs104894331
gopubmedrs104894331
geneviewrs104894331
scholarrs104894331
googlers104894331
pharmgkbrs104894331
gwascentralrs104894331
openSNPrs104894331
23andMers104894331
23andMe allrs104894331
SNP Nexus

SNPshotrs104894331
SNPdbers104894331
MSV3drs104894331
GWAS Ctlgrs104894331
Max Magnitude0
OMIM107777
Desc
Variant0008
Relatedalso
ClinVar
Risk rs104894331(C,G;C,G)
Alt rs104894331(C,G;C,G)
Reference rs104894331(A;A)
Significance Pathogenic
Disease Diabetes insipidus
Variation info
Gene LOC101927318 AQP2
CLNDBN Diabetes insipidus, nephrogenic, autosomal recessive
Reversed 0
HGVS NC_000012.11:g.50344816A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019412.29,