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rs137853867

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853867(A;A)
Make rs137853867(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position64160103
GenePPIB
is asnp
is mentioned by
dbSNPrs137853867
dbSNP (old)rs137853867
ClinGenrs137853867
ebirs137853867
HLIrs137853867
Exacrs137853867
Gnomadrs137853867
Varsomers137853867
Maprs137853867
PheGenIrs137853867
Biobankrs137853867
1000 genomesrs137853867
hgdprs137853867
ensemblrs137853867
gopubmedrs137853867
geneviewrs137853867
scholarrs137853867
googlers137853867
pharmgkbrs137853867
gwascentralrs137853867
openSNPrs137853867
23andMers137853867
23andMe allrs137853867
SNPshotrs137853867
SNPdbers137853867
MSV3drs137853867
GWAS Ctlgrs137853867
Max Magnitude0
ClinVar
Risk rs137853867(A;A)
Alt rs137853867(A;A)
Reference Rs137853867(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PPIB
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.64452302C>T
CLNSRC
CLNACC RCV000024539.1,