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rs767103943

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767103943(A;A)
Make rs767103943(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position9840238
GeneRPUSD3
is asnp
is mentioned by
dbSNPrs767103943
ebirs767103943
HLIrs767103943
Exacrs767103943
Varsomers767103943
Maprs767103943
PheGenIrs767103943
hapmaprs767103943
1000 genomesrs767103943
hgdprs767103943
ensemblrs767103943
gopubmedrs767103943
geneviewrs767103943
scholarrs767103943
googlers767103943
pharmgkbrs767103943
gwascentralrs767103943
openSNPrs767103943
23andMers767103943
23andMe allrs767103943
SNP Nexus

SNPshotrs767103943
SNPdbers767103943
MSV3drs767103943
GWAS Ctlgrs767103943
Max Magnitude0
ClinVar
Risk rs767103943(A;A)
Alt rs767103943(A;A)
Reference rs767103943(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene RPUSD3
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000003.11:g.9881922G>A
CLNSRC
CLNACC RCV000210726.1,