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rs1057520687

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520687(C;C)
Make rs1057520687(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position66866191
GenePC
is asnp
is mentioned by
dbSNPrs1057520687
dbSNP (old)rs1057520687
ClinGenrs1057520687
ebirs1057520687
HLIrs1057520687
Exacrs1057520687
Gnomadrs1057520687
Varsomers1057520687
LitVarrs1057520687
Maprs1057520687
PheGenIrs1057520687
Biobankrs1057520687
1000 genomesrs1057520687
hgdprs1057520687
ensemblrs1057520687
gopubmedrs1057520687
geneviewrs1057520687
scholarrs1057520687
googlers1057520687
pharmgkbrs1057520687
gwascentralrs1057520687
openSNPrs1057520687
23andMers1057520687
23andMe allrs1057520687
SNPshotrs1057520687
SNPdbers1057520687
MSV3drs1057520687
GWAS Ctlgrs1057520687
Max Magnitude0
ClinVar
Risk rs1057520687(C;C)
Alt rs1057520687(C;C)
Reference Rs1057520687(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PC
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.66633662A>G
CLNSRC
CLNACC RCV000433773.1,