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rs2195987

From SNPedia

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Make rs2195987(C;C)
Make rs2195987(C;T)
Make rs2195987(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position23966743
is asnp
is mentioned by
dbSNPrs2195987
ebirs2195987
HLIrs2195987
Exacrs2195987
Varsomers2195987
Maprs2195987
PheGenIrs2195987
hapmaprs2195987
1000 genomesrs2195987
hgdprs2195987
ensemblrs2195987
gopubmedrs2195987
geneviewrs2195987
scholarrs2195987
googlers2195987
pharmgkbrs2195987
gwascentralrs2195987
openSNPrs2195987
23andMers2195987
23andMe allrs2195987
SNP Nexus

SNPshotrs2195987
SNPdbers2195987
MSV3drs2195987
GWAS Ctlgrs2195987
Max Magnitude
? (C;C) (C;T) (T;T) 28
This SNP was reported in [PMID 26503584] as previously discovered in a GWAS experiment as being (slightly) associated with risk for testicular cancer; see that page for it's incorporation in a polygenic risk score.