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rs74315364

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315364(G;T)
Make rs74315364(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position182586014
GeneRNASEL
is asnp
is mentioned by
dbSNPrs74315364
ebirs74315364
HLIrs74315364
Exacrs74315364
Varsomers74315364
Maprs74315364
PheGenIrs74315364
hapmaprs74315364
1000 genomesrs74315364
hgdprs74315364
ensemblrs74315364
gopubmedrs74315364
geneviewrs74315364
scholarrs74315364
googlers74315364
pharmgkbrs74315364
gwascentralrs74315364
openSNPrs74315364
23andMers74315364
23andMe allrs74315364
SNP Nexus

SNPshotrs74315364
SNPdbers74315364
MSV3drs74315364
GWAS Ctlgrs74315364
GMAF0.002296
Max Magnitude0
OMIM180435
Desc
Variant0001
Relatedalso
ClinVar
Risk rs74315364(T;T)
Alt rs74315364(T;T)
Reference rs74315364(G;G)
Significance Pathogenic
Disease Prostate cancer
Variation info
Gene RNASEL
CLNDBN Prostate cancer, hereditary, 1
Reversed 1
HGVS NC_000001.10:g.182555149C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013878.24,