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rs1057517662

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517662(A;A)
Make rs1057517662(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position151667555
GeneSPARC
is asnp
is mentioned by
dbSNPrs1057517662
dbSNP (old)rs1057517662
ClinGenrs1057517662
ebirs1057517662
HLIrs1057517662
Exacrs1057517662
Gnomadrs1057517662
Varsomers1057517662
Maprs1057517662
PheGenIrs1057517662
Biobankrs1057517662
1000 genomesrs1057517662
hgdprs1057517662
ensemblrs1057517662
gopubmedrs1057517662
geneviewrs1057517662
scholarrs1057517662
googlers1057517662
pharmgkbrs1057517662
gwascentralrs1057517662
openSNPrs1057517662
23andMers1057517662
23andMe allrs1057517662
SNPshotrs1057517662
SNPdbers1057517662
MSV3drs1057517662
GWAS Ctlgrs1057517662
Max Magnitude0
ClinVar
Risk rs1057517662(A;A)
Alt rs1057517662(A;A)
Reference Rs1057517662(G;G)
Significance Pathogenic
Disease Osteogenesis imperfecta
Variation info
Gene SPARC
CLNDBN Osteogenesis imperfecta, type xvii
Reversed 1
HGVS NC_000005.9:g.151047116C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000412625.1,