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rs74315365

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315365(A;A)
Make rs74315365(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position182586804
GeneRNASEL
is asnp
is mentioned by
dbSNPrs74315365
ebirs74315365
HLIrs74315365
Exacrs74315365
Varsomers74315365
Maprs74315365
PheGenIrs74315365
hapmaprs74315365
1000 genomesrs74315365
hgdprs74315365
ensemblrs74315365
gopubmedrs74315365
geneviewrs74315365
scholarrs74315365
googlers74315365
pharmgkbrs74315365
gwascentralrs74315365
openSNPrs74315365
23andMers74315365
23andMe allrs74315365
SNP Nexus

SNPshotrs74315365
SNPdbers74315365
MSV3drs74315365
GWAS Ctlgrs74315365
Max Magnitude0
OMIM180435
Desc
Variant0002
Relatedalso
ClinVar
Risk rs74315365(A;A)
Alt rs74315365(A;A)
Reference rs74315365(G;G)
Significance Pathogenic
Disease Prostate cancer
Variation info
Gene RNASEL
CLNDBN Prostate cancer, hereditary, 1
Reversed 1
HGVS NC_000001.10:g.182555939C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013879.23,