rs4792311

plus

Geno	Mag	Summary
(A;A)	2	Increased risk of prostate cancer
(A;G)	2	Increased risk of prostate cancer
(G;G)	1	Normal risk of prostate cancer

Reference

GRCh38 38.1/141

Chromosome

17

Position

13011692

Gene

ELAC2

is a	snp
is	mentioned by
dbSNP	rs4792311
dbSNP (classic)	rs4792311
ClinGen	rs4792311
ebi	rs4792311
HLI	rs4792311
Exac	rs4792311
Gnomad	rs4792311
Varsome	rs4792311
LitVar	rs4792311
Map	rs4792311
PheGenI	rs4792311
Biobank	rs4792311
1000 genomes	rs4792311
hgdp	rs4792311
ensembl	rs4792311
geneview	rs4792311
scholar	rs4792311
google	rs4792311
pharmgkb	rs4792311
gwascentral	rs4792311
openSNP	rs4792311
23andMe	rs4792311
SNPshot	rs4792311
SNPdbe	rs4792311
MSV3d	rs4792311
GWAS Ctlg	rs4792311

GMAF

0.2066

Max Magnitude

2

?

(A;A) (A;G) (G;G)

28

OMIM	605367
Desc	PROSTATE CANCER, SUSCEPTIBILITY TO
Variant	0001
Related	also

ClinVar
Risk	Rs4792311(A;A)
Alt	Rs4792311(A;A)
Reference	Rs4792311(G;G)
Significance	Pathogenic
Disease	Prostate cancer not specified
Variation	info
Gene	ELAC2
CLNDBN	Prostate cancer, hereditary, 2 not specified
Reversed	0
HGVS	NC_000017.10:g.12915009G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005358.3, RCV000419055.1,

[PMID 18375959 ] Sequence variants of elaC homolog 2 (Escherichia coli) (ELAC2) gene and susceptibility to prostate cancer in the Health Professionals Follow-Up Study.

[PMID 19379518 ] Development of a fingerprinting panel using medically relevant polymorphisms.

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

[PMID 20565774 ] Population based allele frequencies of disease associated polymorphisms in the Personalized Medicine Research Project.

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