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rs627928

From SNPedia

Orientationminus
Stabilizedminus
Make rs627928(G;G)
Make rs627928(G;T)
Make rs627928(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position182582202
GeneRNASEL
is asnp
is mentioned by
dbSNPrs627928
ebirs627928
HLIrs627928
Exacrs627928
Varsomers627928
Maprs627928
PheGenIrs627928
hapmaprs627928
1000 genomesrs627928
hgdprs627928
ensemblrs627928
gopubmedrs627928
geneviewrs627928
scholarrs627928
googlers627928
pharmgkbrs627928
gwascentralrs627928
openSNPrs627928
23andMers627928
23andMe allrs627928
SNP Nexus

SNPshotrs627928
SNPdbers627928
MSV3drs627928
GWAS Ctlgrs627928
GMAF0.4743
Max Magnitude
? (G;G) (G;T) (T;T) 28


Venter snp
Source plos
Gene RNASEL
allele C
frequency 0.375
sift
HuRef 1103675278107
Disease Association Defects in RNASEL may be the cause of susceptibility to hereditary prostate cancer 1 (HPC1) (MIM:176807, 601518).



[PMID 18575592OA-icon.png] Germline mutation in RNASEL predicts increased risk of head and neck, uterine cervix and breast cancer.


[PMID 19567509OA-icon.png] Genetic variants and prostate cancer risk: candidate replication and exploration of viral restriction genes.


GET Evidence
RNASEL-D541E
aa_change Asp541Glu
aa_change_short D541E
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.474809
summary