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

rs142932960

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142932960(A;A)
Make rs142932960(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position9839148
GeneRPUSD3
is asnp
is mentioned by
dbSNPrs142932960
ebirs142932960
HLIrs142932960
Exacrs142932960
Varsomers142932960
Maprs142932960
PheGenIrs142932960
hapmaprs142932960
1000 genomesrs142932960
hgdprs142932960
ensemblrs142932960
gopubmedrs142932960
geneviewrs142932960
scholarrs142932960
googlers142932960
pharmgkbrs142932960
gwascentralrs142932960
openSNPrs142932960
23andMers142932960
23andMe allrs142932960
SNP Nexus

SNPshotrs142932960
SNPdbers142932960
MSV3drs142932960
GWAS Ctlgrs142932960
Max Magnitude0
ClinVar
Risk rs142932960(A;A)
Alt rs142932960(A;A)
Reference rs142932960(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene RPUSD3
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000003.11:g.9880832G>A
CLNSRC
CLNACC RCV000210730.1,