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rs1057521972

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521972(C;C)
Make rs1057521972(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position87612104
GeneDSPP
is asnp
is mentioned by
dbSNPrs1057521972
dbSNP (old)rs1057521972
ClinGenrs1057521972
ebirs1057521972
HLIrs1057521972
Exacrs1057521972
Gnomadrs1057521972
Varsomers1057521972
LitVarrs1057521972
Maprs1057521972
PheGenIrs1057521972
Biobankrs1057521972
1000 genomesrs1057521972
hgdprs1057521972
ensemblrs1057521972
gopubmedrs1057521972
geneviewrs1057521972
scholarrs1057521972
googlers1057521972
pharmgkbrs1057521972
gwascentralrs1057521972
openSNPrs1057521972
23andMers1057521972
23andMe allrs1057521972
SNPshotrs1057521972
SNPdbers1057521972
MSV3drs1057521972
GWAS Ctlgrs1057521972
Max Magnitude0
ClinVar
Risk rs1057521972(C;C)
Alt rs1057521972(C;C)
Reference Rs1057521972(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSPP
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.88533256G>C
CLNSRC
CLNACC RCV000419635.1,