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rs878855044

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855044(A;A)
Make rs878855044(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position70435285
GeneNODAL
is asnp
is mentioned by
dbSNPrs878855044
ebirs878855044
HLIrs878855044
Exacrs878855044
Varsomers878855044
Maprs878855044
PheGenIrs878855044
hapmaprs878855044
1000 genomesrs878855044
hgdprs878855044
ensemblrs878855044
gopubmedrs878855044
geneviewrs878855044
scholarrs878855044
googlers878855044
pharmgkbrs878855044
gwascentralrs878855044
openSNPrs878855044
23andMers878855044
23andMe allrs878855044
SNP Nexus

SNPshotrs878855044
SNPdbers878855044
MSV3drs878855044
GWAS Ctlgrs878855044
Max Magnitude0
ClinVar
Risk rs878855044(A;A)
Alt rs878855044(A;A)
Reference rs878855044(G;G)
Significance Probable-Pathogenic
Disease Visceral heterotaxy 5
Variation info
Gene NODAL
CLNDBN Visceral heterotaxy 5, autosomal
Reversed 1
HGVS NC_000010.10:g.72195041C>T
CLNSRC
CLNACC RCV000231796.1,