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rs137853865

From SNPedia

Orientationminus
Make rs137853865(-;-)
Make rs137853865(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position64162867
GenePPIB
is asnp
is mentioned by
dbSNPrs137853865
ebirs137853865
HLIrs137853865
Exacrs137853865
Varsomers137853865
Maprs137853865
PheGenIrs137853865
hapmaprs137853865
1000 genomesrs137853865
hgdprs137853865
ensemblrs137853865
gopubmedrs137853865
geneviewrs137853865
scholarrs137853865
googlers137853865
pharmgkbrs137853865
gwascentralrs137853865
openSNPrs137853865
23andMers137853865
23andMe allrs137853865
SNP Nexus

SNPshotrs137853865
SNPdbers137853865
MSV3drs137853865
GWAS Ctlgrs137853865
Max Magnitude
ClinVar
Risk rs137853865(;)
Alt rs137853865(;)
Reference rs137853865(C;C)
Significance Pathogenic
Disease not provided Osteogenesis imperfecta type 9
Variation info
Gene PPIB
CLNDBN not provided Osteogenesis imperfecta type 9
Reversed 1
HGVS NC_000015.9:g.64455066delG
CLNSRC OMIM Allelic Variant Osteogenesis Imperfecta Variant Database (PPIB)
CLNACC RCV000024537.1, RCV000202411.1,