Have questions? Visit https://www.reddit.com/r/SNPedia

rs1559806

From SNPedia

Orientationminus
Stabilizedminus
Make rs1559806(C;C)
Make rs1559806(C;T)
Make rs1559806(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position74441552
GeneFAM69C
is asnp
is mentioned by
dbSNPrs1559806
ebirs1559806
HLIrs1559806
Exacrs1559806
Varsomers1559806
Maprs1559806
PheGenIrs1559806
hapmaprs1559806
1000 genomesrs1559806
hgdprs1559806
ensemblrs1559806
gopubmedrs1559806
geneviewrs1559806
scholarrs1559806
googlers1559806
pharmgkbrs1559806
gwascentralrs1559806
openSNPrs1559806
23andMers1559806
23andMe allrs1559806
SNP Nexus

SNPshotrs1559806
SNPdbers1559806
MSV3drs1559806
GWAS Ctlgrs1559806
GMAF0.4867
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22615748OA-icon.png] Absence of XMRV and Closely Related Viruses in Primary Prostate Cancer Tissues Used to Derive the XMRV-Infected Cell Line 22Rv1