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rs1057517870

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517870(C;T)
Make rs1057517870(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position19186266
GeneCSRP3
is asnp
is mentioned by
dbSNPrs1057517870
dbSNP (classic)rs1057517870
ClinGenrs1057517870
ebirs1057517870
HLIrs1057517870
Exacrs1057517870
Gnomadrs1057517870
Varsomers1057517870
LitVarrs1057517870
Maprs1057517870
PheGenIrs1057517870
Biobankrs1057517870
1000 genomesrs1057517870
hgdprs1057517870
ensemblrs1057517870
geneviewrs1057517870
scholarrs1057517870
googlers1057517870
pharmgkbrs1057517870
gwascentralrs1057517870
openSNPrs1057517870
23andMers1057517870
23andMe allrs1057517870
SNPshotrs1057517870
SNPdbers1057517870
MSV3drs1057517870
GWAS Ctlgrs1057517870
Max Magnitude0
ClinVar
Risk rs1057517870(T;T)
Alt rs1057517870(T;T)
Reference Rs1057517870(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CSRP3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.19207813G>A
CLNSRC
CLNACC RCV000413421.1,