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rs765004815

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs765004815(A;A)
Make rs765004815(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position4874766
GeneUBN1
is asnp
is mentioned by
dbSNPrs765004815
ebirs765004815
HLIrs765004815
Exacrs765004815
Varsomers765004815
Maprs765004815
PheGenIrs765004815
hapmaprs765004815
1000 genomesrs765004815
hgdprs765004815
ensemblrs765004815
gopubmedrs765004815
geneviewrs765004815
scholarrs765004815
googlers765004815
pharmgkbrs765004815
gwascentralrs765004815
openSNPrs765004815
23andMers765004815
23andMe allrs765004815
SNP Nexus

SNPshotrs765004815
SNPdbers765004815
MSV3drs765004815
GWAS Ctlgrs765004815
Max Magnitude0
ClinVar
Risk rs765004815(A;A)
Alt rs765004815(A;A)
Reference rs765004815(T;T)
Significance Probable-Pathogenic
Disease Non-immune hydrops fetalis
Variation info
Gene UBN1
CLNDBN Non-immune hydrops fetalis
Reversed 0
HGVS NC_000016.9:g.4924767T>A
CLNSRC
CLNACC RCV000170572.1,