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rs1057517663

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517663(A;A)
Make rs1057517663(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position151664183
GeneSPARC
is asnp
is mentioned by
dbSNPrs1057517663
dbSNP (old)rs1057517663
ClinGenrs1057517663
ebirs1057517663
HLIrs1057517663
Exacrs1057517663
Gnomadrs1057517663
Varsomers1057517663
Maprs1057517663
PheGenIrs1057517663
Biobankrs1057517663
1000 genomesrs1057517663
hgdprs1057517663
ensemblrs1057517663
gopubmedrs1057517663
geneviewrs1057517663
scholarrs1057517663
googlers1057517663
pharmgkbrs1057517663
gwascentralrs1057517663
openSNPrs1057517663
23andMers1057517663
23andMe allrs1057517663
SNPshotrs1057517663
SNPdbers1057517663
MSV3drs1057517663
GWAS Ctlgrs1057517663
Max Magnitude0
ClinVar
Risk rs1057517663(A;A)
Alt rs1057517663(A;A)
Reference Rs1057517663(G;G)
Significance Pathogenic
Disease Osteogenesis imperfecta
Variation info
Gene SPARC
CLNDBN Osteogenesis imperfecta, type xvii
Reversed 1
HGVS NC_000005.9:g.151043744C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000412523.1,