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rs878853079

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853079(C;C)
Make rs878853079(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153905898
GeneAVPR2
is asnp
is mentioned by
dbSNPrs878853079
ebirs878853079
HLIrs878853079
Exacrs878853079
Varsomers878853079
Maprs878853079
PheGenIrs878853079
hapmaprs878853079
1000 genomesrs878853079
hgdprs878853079
ensemblrs878853079
gopubmedrs878853079
geneviewrs878853079
scholarrs878853079
googlers878853079
pharmgkbrs878853079
gwascentralrs878853079
openSNPrs878853079
23andMers878853079
23andMe allrs878853079
SNP Nexus

SNPshotrs878853079
SNPdbers878853079
MSV3drs878853079
GWAS Ctlgrs878853079
Max Magnitude0
ClinVar
Risk rs878853079(C;C)
Alt rs878853079(C;C)
Reference rs878853079(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene AVPR2
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153171352T>C
CLNSRC
CLNACC RCV000224807.1,