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Difference between revisions of "Rs508485"

From SNPedia
m (Text replace - "{{on chip | FTDNA2}}" to "")
m (Set on chip)
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{{on chip | 23andMe v3}}
 
{{on chip | 23andMe v3}}
 
{{on chip | Affy GenomeWide 6}}
 
{{on chip | Affy GenomeWide 6}}
 
+
{{on chip | FTDNA2}}
 
{{on chip | FTDNA}}
 
{{on chip | FTDNA}}
 
{{on chip | HumanOmni1Quad}}
 
{{on chip | HumanOmni1Quad}}
 
{{on chip | Illumina Human 1M}}
 
{{on chip | Illumina Human 1M}}

Revision as of 09:33, 6 September 2011

Orientationplus
Make rs508485(C;C)
Make rs508485(C;T)
Make rs508485(T;T)
ReferenceGRCh37 37.1/132
Chromosome11
Position94354479
GenePIWIL4
is asnp
is mentioned by
dbSNPrs508485
dbSNP (classic)rs508485
ClinGenrs508485
ebirs508485
HLIrs508485
Exacrs508485
Gnomadrs508485
Varsomers508485
LitVarrs508485
Maprs508485
PheGenIrs508485
Biobankrs508485
1000 genomesrs508485
hgdprs508485
ensemblrs508485
geneviewrs508485
scholarrs508485
googlers508485
pharmgkbrs508485
gwascentralrs508485
openSNPrs508485
23andMers508485
SNPshotrs508485
SNPdbers508485
MSV3drs508485
GWAS Ctlgrs508485
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 20940137] Genetic variants in Piwi-interacting RNA pathway genes confer susceptibility to spermatogenic failure in a Chinese population