rs121912582

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121912582(C;T)

Make rs121912582(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

22907980

Gene

EPHB2

is a	snp
is	mentioned by
dbSNP	rs121912582
dbSNP (classic)	rs121912582
ClinGen	rs121912582
ebi	rs121912582
HLI	rs121912582
Exac	rs121912582
Gnomad	rs121912582
Varsome	rs121912582
LitVar	rs121912582
Map	rs121912582
PheGenI	rs121912582
Biobank	rs121912582
1000 genomes	rs121912582
hgdp	rs121912582
ensembl	rs121912582
geneview	rs121912582
scholar	rs121912582
google	rs121912582
pharmgkb	rs121912582
gwascentral	rs121912582
openSNP	rs121912582
23andMe	rs121912582
SNPshot	rs121912582
SNPdbe	rs121912582
MSV3d	rs121912582
GWAS Ctlg	rs121912582

Max Magnitude

0

OMIM	600997
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121912582(T;T)
Alt	rs121912582(T;T)
Reference	Rs121912582(C;C)
Significance	Pathogenic
Disease	Prostate cancer/brain cancer susceptibility
Variation	info
Gene	EPHB2
CLNDBN	Prostate cancer/brain cancer susceptibility
Reversed	0
HGVS	NC_000001.10:g.23234473C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009058.6,