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rs370243877

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs370243877(A;T)
Make rs370243877(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position47941773
GenePNPO, SP2-AS1
is asnp
is mentioned by
dbSNPrs370243877
ebirs370243877
HLIrs370243877
Exacrs370243877
Varsomers370243877
Maprs370243877
PheGenIrs370243877
hapmaprs370243877
1000 genomesrs370243877
hgdprs370243877
ensemblrs370243877
gopubmedrs370243877
geneviewrs370243877
scholarrs370243877
googlers370243877
pharmgkbrs370243877
gwascentralrs370243877
openSNPrs370243877
23andMers370243877
23andMe allrs370243877
SNP Nexus

SNPshotrs370243877
SNPdbers370243877
MSV3drs370243877
GWAS Ctlgrs370243877
Max Magnitude0
ClinVar
Risk rs370243877(T;T)
Alt rs370243877(T;T)
Reference rs370243877(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC100506325 SP2-AS1 PNPO
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.46019139A>T
CLNSRC
CLNACC RCV000188506.2,