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rs878855322

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs878855322(-;-)
Make rs878855322(-;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position77029529
GenePSTPIP1
is asnp
is mentioned by
dbSNPrs878855322
ebirs878855322
HLIrs878855322
Exacrs878855322
Varsomers878855322
Maprs878855322
PheGenIrs878855322
hapmaprs878855322
1000 genomesrs878855322
hgdprs878855322
ensemblrs878855322
gopubmedrs878855322
geneviewrs878855322
scholarrs878855322
googlers878855322
pharmgkbrs878855322
gwascentralrs878855322
openSNPrs878855322
23andMers878855322
23andMe allrs878855322
SNP Nexus

SNPshotrs878855322
SNPdbers878855322
MSV3drs878855322
GWAS Ctlgrs878855322
Max Magnitude0
ClinVar
Risk rs878855322(;)
Alt rs878855322(;)
Reference rs878855322(AG;AG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PSTPIP1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.77321870_77321871delAG
CLNSRC
CLNACC RCV000231956.1,