Have questions? Visit https://www.reddit.com/r/SNPedia

rs387906327

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906327(-;-)
Make rs387906327(-;G)
Make rs387906327(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position12996564
GeneELAC2
is asnp
is mentioned by
dbSNPrs387906327
ebirs387906327
HLIrs387906327
Exacrs387906327
Varsomers387906327
Maprs387906327
PheGenIrs387906327
hapmaprs387906327
1000 genomesrs387906327
hgdprs387906327
ensemblrs387906327
gopubmedrs387906327
geneviewrs387906327
scholarrs387906327
googlers387906327
pharmgkbrs387906327
gwascentralrs387906327
openSNPrs387906327
23andMers387906327
23andMe allrs387906327
SNP Nexus

SNPshotrs387906327
SNPdbers387906327
MSV3drs387906327
GWAS Ctlgrs387906327
Max Magnitude0
ClinVar
Risk rs387906327(G;G)
Alt rs387906327(G;G)
Reference rs387906327(;)
Significance Pathogenic
Disease Prostate cancer
Variation info
Gene ELAC2
CLNDBN Prostate cancer, hereditary, 2
Reversed 1
HGVS NC_000017.10:g.12899882dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000005360.2,