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rs11545302

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs11545302(A;G)
Make rs11545302(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position12996646
GeneELAC2
is asnp
is mentioned by
dbSNPrs11545302
dbSNP (classic)rs11545302
ClinGenrs11545302
ebirs11545302
HLIrs11545302
Exacrs11545302
Gnomadrs11545302
Varsomers11545302
LitVarrs11545302
Maprs11545302
PheGenIrs11545302
Biobankrs11545302
1000 genomesrs11545302
hgdprs11545302
ensemblrs11545302
geneviewrs11545302
scholarrs11545302
googlers11545302
pharmgkbrs11545302
gwascentralrs11545302
openSNPrs11545302
23andMers11545302
SNPshotrs11545302
SNPdbers11545302
MSV3drs11545302
GWAS Ctlgrs11545302
Max Magnitude0

[PMID 27318894] Association between RNASEL, MSR1, and ELAC2 single nucleotide polymorphisms and gene expression in prostate cancer risk.

ClinVar
Risk rs11545302(G;G) rs11545302(T;T)
Alt rs11545302(G;G) rs11545302(T;T)
Reference Rs11545302(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ELAC2
CLNDBN not specified
Reversed 1
HGVS NC_000017.10:g.12899963T>C
CLNSRC
CLNACC RCV000434605.1,