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

rs796052096

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052096(A;T)
Make rs796052096(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153905894
GeneAVPR2
is asnp
is mentioned by
dbSNPrs796052096
ClinGenrs796052096
ebirs796052096
HLIrs796052096
Exacrs796052096
Varsomers796052096
Maprs796052096
PheGenIrs796052096
hapmaprs796052096
1000 genomesrs796052096
hgdprs796052096
ensemblrs796052096
gopubmedrs796052096
geneviewrs796052096
scholarrs796052096
googlers796052096
pharmgkbrs796052096
gwascentralrs796052096
openSNPrs796052096
23andMers796052096
23andMe allrs796052096
SNP Nexus

SNPshotrs796052096
SNPdbers796052096
MSV3drs796052096
GWAS Ctlgrs796052096
Max Magnitude0
ClinVar
Risk rs796052096(T;T)
Alt rs796052096(T;T)
Reference Rs796052096(A;A)
Significance Pathogenic
Disease Nephrogenic diabetes insipidus
Variation info
Gene AVPR2
CLNDBN Nephrogenic diabetes insipidus, X-linked
Reversed 0
HGVS NC_000023.10:g.153171348A>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000186513.2,