rs76826147

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in complete genomics

Make rs76826147(A;T)

Make rs76826147(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

22913757

Gene

EPHB2

is a	snp
is	mentioned by
dbSNP	rs76826147
dbSNP (classic)	rs76826147
ClinGen	rs76826147
ebi	rs76826147
HLI	rs76826147
Exac	rs76826147
Gnomad	rs76826147
Varsome	rs76826147
LitVar	rs76826147
Map	rs76826147
PheGenI	rs76826147
Biobank	rs76826147
1000 genomes	rs76826147
hgdp	rs76826147
ensembl	rs76826147
geneview	rs76826147
scholar	rs76826147
google	rs76826147
pharmgkb	rs76826147
gwascentral	rs76826147
openSNP	rs76826147
23andMe	rs76826147
SNPshot	rs76826147
SNPdbe	rs76826147
MSV3d	rs76826147
GWAS Ctlg	rs76826147

GMAF

0.0124

Max Magnitude

0

OMIM	600997
Desc
Variant	0004
Related	also

ClinVar
Risk	rs76826147(G;G) rs76826147(T;T)
Alt	rs76826147(G;G) rs76826147(T;T)
Reference	Rs76826147(A;A)
Significance	Other
Disease	Prostate cancer/brain cancer susceptibility
Variation	info
Gene	EPHB2
CLNDBN	Prostate cancer/brain cancer susceptibility
Reversed	0
HGVS	NC_000001.10:g.23240250A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009061.4,