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

rs886040961

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886040961(-;-)
Make rs886040961(-;C)
ReferenceGRCh38.p7 38.3/149
ChromosomeX
Position153906578
GeneAVPR2
is asnp
is mentioned by
dbSNPrs886040961
dbSNP (classic)rs886040961
ClinGenrs886040961
ebirs886040961
HLIrs886040961
Exacrs886040961
Gnomadrs886040961
Varsomers886040961
LitVarrs886040961
Maprs886040961
PheGenIrs886040961
Biobankrs886040961
1000 genomesrs886040961
hgdprs886040961
ensemblrs886040961
geneviewrs886040961
scholarrs886040961
googlers886040961
pharmgkbrs886040961
gwascentralrs886040961
openSNPrs886040961
23andMers886040961
SNPshotrs886040961
SNPdbers886040961
MSV3drs886040961
GWAS Ctlgrs886040961
Max Magnitude0
ClinVar
Risk rs886040961(-;-)
Alt rs886040961(-;-)
Reference Rs886040961(C;C)
Significance Pathogenic
Disease Nephrogenic diabetes insipidus
Variation info
Gene AVPR2
CLNDBN Nephrogenic diabetes insipidus, X-linked
Reversed 0
HGVS NC_000023.10:g.153172032delC
CLNSRC
CLNACC RCV000258016.1,