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rs142012387

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142012387(G;T)
Make rs142012387(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position70600460
GenePRF1
is asnp
is mentioned by
dbSNPrs142012387
dbSNP (old)rs142012387
ClinGenrs142012387
ebirs142012387
HLIrs142012387
Exacrs142012387
Gnomadrs142012387
Varsomers142012387
Maprs142012387
PheGenIrs142012387
Biobankrs142012387
1000 genomesrs142012387
hgdprs142012387
ensemblrs142012387
gopubmedrs142012387
geneviewrs142012387
scholarrs142012387
googlers142012387
pharmgkbrs142012387
gwascentralrs142012387
openSNPrs142012387
23andMers142012387
23andMe allrs142012387
SNPshotrs142012387
SNPdbers142012387
MSV3drs142012387
GWAS Ctlgrs142012387
Max Magnitude0
ClinVar
Risk rs142012387(C;C) rs142012387(T;T)
Alt rs142012387(C;C) rs142012387(T;T)
Reference Rs142012387(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PRF1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.72360216G>C
CLNSRC
CLNACC RCV000424261.1,